Linked Data
ClinVar Variation Id:
93543
dbSNP Id:
rs76956936
ExAC:
18:52895549 C / T
gnomAD v2:
18-52895549-C-T
gnomAD v3:
18-55228318-C-T
gnomAD v4:
18-55228318-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.55228318C>T , CM000680.2:g.55228318C>T | GRCh38 |
| NC_000018.9:g.52895549C>T , CM000680.1:g.52895549C>T | GRCh37 |
| NC_000018.8:g.51046547C>T | NCBI36 |
| NG_011716.1:g.365312G>A | |
| NG_011716.2:g.412676G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354452.8:c.1923G>A MANE Select | ENSP00000346440.3:p.Glu641= | |
| ENST00000635822.2:c.1803G>A | ENSP00000490451.1:p.Glu601= | |
| ENST00000635990.2:n.1603G>A | ||
| ENST00000636400.2:c.1851G>A | ENSP00000490006.1:p.Glu617= | |
| ENST00000636751.2:c.*1631G>A | ENSP00000489783.1:n.*1631G>A | |
| ENST00000636822.2:c.1533G>A | ENSP00000490883.1:p.Glu511= | |
| ENST00000637115.2:c.*1801G>A | ENSP00000490234.1:n.*1801G>A | |
| ENST00000637169.2:c.1275G>A | ENSP00000490832.1:p.Glu425= | |
| ENST00000637239.2:n.1978G>A | ||
| ENST00000637250.2:n.1617G>A | ||
| ENST00000637923.2:c.1521G>A | ||
| ENST00000638154.3:c.1950G>A | ENSP00000490625.2:p.Glu650= | |
| ENST00000643689.1:c.1533G>A | ENSP00000494380.1:p.Glu511= | |
| ENST00000674764.1:c.*1534G>A | ENSP00000502213.1:n.*1534G>A | |
| ENST00000675707.1:c.1533G>A | ENSP00000501758.1:p.Glu511= | |
| ENST00000354452.7:c.1923G>A | ENSP00000346440.3:p.Glu641= | |
| ENST00000356073.8:c.1911G>A | ENSP00000348374.4:p.Glu637= | |
| ENST00000398339.5:c.2229G>A | ENSP00000381382.1:p.Glu743= | |
| ENST00000457482.7:c.1443G>A | ENSP00000409447.2:p.Glu481= | |
| ENST00000537578.5:c.1851G>A | ENSP00000440731.1:p.Glu617= | |
| ENST00000537856.7:c.1521G>A | ENSP00000439827.2:p.Glu507= | |
| ENST00000540999.5:c.1839G>A | ENSP00000445202.1:p.Glu613= | |
| ENST00000543082.5:c.1785G>A | ENSP00000439656.1:p.Glu595= | |
| ENST00000544241.6:c.1710G>A | ENSP00000441562.2:p.Glu570= | |
| ENST00000561831.7:c.1431G>A | ENSP00000457765.1:p.Glu477= | |
| ENST00000561992.5:c.1521G>A | ENSP00000455179.1:p.Glu507= | |
| ENST00000562680.5:n.5446G>A | ||
| ENST00000564228.5:c.1698G>A | ENSP00000455261.1:p.Glu566= | |
| ENST00000564403.6:c.1941G>A | ENSP00000457263.1:p.Glu647= | |
| ENST00000564999.5:c.1911G>A | ENSP00000457649.1:p.Glu637= | |
| ENST00000565018.6:c.1659G>A | ENSP00000455984.2:p.Glu553= | |
| ENST00000566279.5:c.1743G>A | ENSP00000456125.1:p.Glu581= | |
| ENST00000566286.5:c.1902G>A | ENSP00000455418.2:p.Glu634= | |
| ENST00000567880.5:c.1731G>A | ENSP00000454366.1:p.Glu577= | |
| ENST00000568673.5:c.1851G>A | ENSP00000455135.1:p.Glu617= | |
| ENST00000568740.5:c.1836G>A | ENSP00000455346.1:p.Glu612= | |
| ENST00000570177.6:c.1521G>A | ENSP00000454647.1:p.Glu507= | |
| ENST00000570287.6:c.1431G>A | ENSP00000455763.1:p.Glu477= | |
| ENST00000616053.4:c.1659G>A | ENSP00000478549.1:p.Glu553= | |
| ENST00000626466.1:n.946G>A | ||
| ENST00000626584.2:c.1263G>A | ENSP00000486072.1:p.Glu421= | |
| ENST00000626631.1:c.153G>A | ENSP00000487505.1:p.Glu51= | |
| ENST00000629387.2:c.1923G>A | ENSP00000486670.1:p.Glu641= | |
| NM_001083962.1:c.1923G>A | NP_001077431.1:p.Glu641= | |
| NM_001243226.2:c.2229G>A | NP_001230155.2:p.Glu743= | |
| NM_001243227.1:c.1851G>A | NP_001230156.1:p.Glu617= | |
| NM_001243228.1:c.1941G>A | NP_001230157.1:p.Glu647= | |
| NM_001243230.1:c.1902G>A | NP_001230159.1:p.Glu634= | |
| NM_001243231.1:c.1785G>A | NP_001230160.1:p.Glu595= | |
| NM_001243232.1:c.1710G>A | NP_001230161.1:p.Glu570= | |
| NM_001243233.1:c.1521G>A | NP_001230162.1:p.Glu507= | |
| NM_001243234.1:c.1443G>A | NP_001230163.1:p.Glu481= | |
| NM_001243235.1:c.1431G>A | NP_001230164.1:p.Glu477= | |
| NM_001243236.1:c.1431G>A | NP_001230165.1:p.Glu477= | |
| NM_001306207.1:c.1839G>A | NP_001293136.1:p.Glu613= | |
| NM_001306208.1:c.1698G>A | NP_001293137.1:p.Glu566= | |
| NM_003199.2:c.1911G>A | NP_003190.1:p.Glu637= | |
| XM_005266739.3:c.1851G>A | XP_005266796.2:p.Glu617= | |
| XM_005266741.3:c.1920G>A | XP_005266798.1:p.Glu640= | |
| XM_005266743.3:c.1851G>A | XP_005266800.1:p.Glu617= | |
| XM_005266744.3:c.1851G>A | XP_005266801.1:p.Glu617= | |
| XM_005266745.3:c.1848G>A | XP_005266802.1:p.Glu616= | |
| XM_005266747.3:c.1797G>A | XP_005266804.1:p.Glu599= | |
| XM_005266749.3:c.1713G>A | XP_005266806.1:p.Glu571= | |
| XM_005266752.3:c.1533G>A | XP_005266809.1:p.Glu511= | |
| XM_005266754.3:c.1533G>A | XP_005266811.1:p.Glu511= | |
| XM_005266755.3:c.1533G>A | XP_005266812.1:p.Glu511= | |
| XM_005266761.3:c.1440G>A | XP_005266818.1:p.Glu480= | |
| XM_006722536.2:c.1923G>A | XP_006722599.1:p.Glu641= | |
| XM_006722537.2:c.1923G>A | XP_006722600.1:p.Glu641= | |
| XM_006722538.2:c.1848G>A | XP_006722601.1:p.Glu616= | |
| XM_006722539.2:c.1533G>A | XP_006722602.1:p.Glu511= | |
| XM_006722540.2:c.1521G>A | XP_006722603.1:p.Glu507= | |
| XM_011526154.1:c.2226G>A | XP_011524456.1:p.Glu742= | |
| XM_011526155.1:c.2226G>A | XP_011524457.1:p.Glu742= | |
| XM_011526156.1:c.2217G>A | XP_011524458.1:p.Glu739= | |
| XM_011526157.1:c.2214G>A | XP_011524459.1:p.Glu738= | |
| XM_011526158.1:c.1917G>A | XP_011524460.1:p.Glu639= | |
| XM_011526159.1:c.1533G>A | XP_011524461.1:p.Glu511= | |
| XM_011526160.1:c.1533G>A | XP_011524462.1:p.Glu511= | |
| XM_011526161.1:c.1533G>A | XP_011524463.1:p.Glu511= | |
| XM_011526162.1:c.1533G>A | XP_011524464.1:p.Glu511= | |
| XM_011526163.1:c.1533G>A | XP_011524465.1:p.Glu511= | |
| XM_011526164.1:c.1521G>A | XP_011524466.1:p.Glu507= | |
| NM_001330604.2:c.1920G>A | NP_001317533.1:p.Glu640= | |
| NM_001330605.2:c.1533G>A | NP_001317534.1:p.Glu511= | |
| NM_001348211.1:c.1797G>A | NP_001335140.1:p.Glu599= | |
| NM_001348212.1:c.1521G>A | NP_001335141.1:p.Glu507= | |
| NM_001348213.1:c.1533G>A | NP_001335142.1:p.Glu511= | |
| NM_001348214.1:c.1428G>A | NP_001335143.1:p.Glu476= | |
| NM_001348215.1:c.1275G>A | NP_001335144.1:p.Glu425= | |
| NM_001348216.1:c.1443G>A | NP_001335145.1:p.Glu481= | |
| NM_001348217.1:c.1851G>A | NP_001335146.1:p.Glu617= | |
| NM_001348218.1:c.1851G>A | NP_001335147.1:p.Glu617= | |
| NM_001348219.1:c.1839G>A | NP_001335148.1:p.Glu613= | |
| NM_001348220.1:c.1836G>A | NP_001335149.1:p.Glu612= | |
| XM_005266739.4:c.1851G>A | XP_005266796.2:p.Glu617= | |
| XM_005266741.4:c.1920G>A | XP_005266798.1:p.Glu640= | |
| XM_005266745.4:c.1848G>A | XP_005266802.1:p.Glu616= | |
| XM_005266749.4:c.1713G>A | XP_005266806.1:p.Glu571= | |
| XM_005266752.5:c.1533G>A | XP_005266809.1:p.Glu511= | |
| XM_005266755.5:c.1533G>A | XP_005266812.1:p.Glu511= | |
| XM_005266761.4:c.1440G>A | XP_005266818.1:p.Glu480= | |
| XM_006722536.3:c.1923G>A | XP_006722599.1:p.Glu641= | |
| XM_006722537.3:c.1923G>A | XP_006722600.1:p.Glu641= | |
| XM_006722538.3:c.1848G>A | XP_006722601.1:p.Glu616= | |
| XM_017025934.2:c.1848G>A | XP_016881423.1:p.Glu616= | |
| XM_017025935.2:c.1848G>A | XP_016881424.1:p.Glu616= | |
| XM_017025936.2:c.1839G>A | XP_016881425.1:p.Glu613= | |
| XM_017025937.2:c.1836G>A | XP_016881426.1:p.Glu612= | |
| XM_017025938.2:c.1920G>A | XP_016881427.1:p.Glu640= | |
| XM_017025940.2:c.1911G>A | XP_016881429.1:p.Glu637= | |
| XM_017025941.2:c.1911G>A | XP_016881430.1:p.Glu637= | |
| XM_017025942.2:c.1908G>A | XP_016881431.1:p.Glu636= | |
| XM_017025943.2:c.1908G>A | XP_016881432.1:p.Glu636= | |
| XM_017025944.2:c.1848G>A | XP_016881433.1:p.Glu616= | |
| XM_017025945.2:c.1848G>A | XP_016881434.1:p.Glu616= | |
| XM_017025946.2:c.1839G>A | XP_016881435.1:p.Glu613= | |
| XM_017025948.2:c.1836G>A | XP_016881437.1:p.Glu612= | |
| XM_017025950.2:c.1833G>A | XP_016881439.1:p.Glu611= | |
| XM_017025951.2:c.1794G>A | XP_016881440.1:p.Glu598= | |
| XM_017025952.2:c.1707G>A | XP_016881441.1:p.Glu569= | |
| XM_017025953.2:c.1701G>A | XP_016881442.1:p.Glu567= | |
| XM_017025954.2:c.1530G>A | XP_016881443.1:p.Glu510= | |
| XM_017025956.2:c.1521G>A | XP_016881445.1:p.Glu507= | |
| XM_024451240.1:c.1848G>A | XP_024307008.1:p.Glu616= | |
| XM_024451241.1:c.1686G>A | XP_024307009.1:p.Glu562= | |
| NM_001083962.2:c.1923G>A MANE Select | NP_001077431.1:p.Glu641= | |
| NM_001243226.3:c.2229G>A | NP_001230155.2:p.Glu743= | |
| NM_001243227.2:c.1851G>A | NP_001230156.1:p.Glu617= | |
| NM_001243228.2:c.1941G>A | NP_001230157.1:p.Glu647= | |
| NM_001243231.2:c.1785G>A | NP_001230160.1:p.Glu595= | |
| NM_001243233.2:c.1521G>A | NP_001230162.1:p.Glu507= | |
| NM_001243234.2:c.1443G>A | NP_001230163.1:p.Glu481= | |
| NM_001243235.2:c.1431G>A | NP_001230164.1:p.Glu477= | |
| NM_001243236.2:c.1431G>A | NP_001230165.1:p.Glu477= | |
| NM_001330604.3:c.1920G>A | NP_001317533.1:p.Glu640= | |
| NM_001330605.3:c.1533G>A | NP_001317534.1:p.Glu511= | |
| NM_001348211.2:c.1797G>A | NP_001335140.1:p.Glu599= | |
| NM_001348212.2:c.1521G>A | NP_001335141.1:p.Glu507= | |
| NM_001348213.2:c.1533G>A | NP_001335142.1:p.Glu511= | |
| NM_001348214.2:c.1428G>A | NP_001335143.1:p.Glu476= | |
| NM_001348215.2:c.1275G>A | NP_001335144.1:p.Glu425= | |
| NM_001348216.2:c.1443G>A | NP_001335145.1:p.Glu481= | |
| NM_001348218.2:c.1851G>A | NP_001335147.1:p.Glu617= | |
| NM_001348219.2:c.1839G>A | NP_001335148.1:p.Glu613= | |
| NM_001369567.1:c.1923G>A | NP_001356496.1:p.Glu641= | |
| NM_001369568.1:c.1923G>A | NP_001356497.1:p.Glu641= | |
| NM_001369569.1:c.1920G>A | NP_001356498.1:p.Glu640= | |
| NM_001369570.1:c.1920G>A | NP_001356499.1:p.Glu640= | |
| NM_001369571.1:c.1911G>A | NP_001356500.1:p.Glu637= | |
| NM_001369572.1:c.1911G>A | NP_001356501.1:p.Glu637= | |
| NM_001369573.1:c.1908G>A | NP_001356502.1:p.Glu636= | |
| NM_001369574.1:c.1908G>A | NP_001356503.1:p.Glu636= | |
| NM_001369575.1:c.1851G>A | NP_001356504.1:p.Glu617= | |
| NM_001369576.1:c.1848G>A | NP_001356505.1:p.Glu616= | |
| NM_001369577.1:c.1848G>A | NP_001356506.1:p.Glu616= | |
| NM_001369578.1:c.1848G>A | NP_001356507.1:p.Glu616= | |
| NM_001369579.1:c.1848G>A | NP_001356508.1:p.Glu616= | |
| NM_001369580.1:c.1848G>A | NP_001356509.1:p.Glu616= | |
| NM_001369581.1:c.1848G>A | NP_001356510.1:p.Glu616= | |
| NM_001369582.1:c.1839G>A | NP_001356511.1:p.Glu613= | |
| NM_001369583.1:c.1839G>A | NP_001356512.1:p.Glu613= | |
| NM_001369584.1:c.1836G>A | NP_001356513.1:p.Glu612= | |
| NM_001369585.1:c.1836G>A | NP_001356514.1:p.Glu612= | |
| NM_001369586.1:c.1854G>A | NP_001356515.1:p.Glu618= | |
| NM_003199.3:c.1911G>A | NP_003190.1:p.Glu637= | |
| NM_001243230.2:c.1902G>A | NP_001230159.1:p.Glu634= |