Linked Data
ClinVar Variation Id:
413652
dbSNP Id:
rs376306544
ExAC:
16:2137884 C / T
gnomAD v2:
16-2137884-C-T
gnomAD v3:
16-2087883-C-T
gnomAD v4:
16-2087883-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2087883C>T , CM000678.2:g.2087883C>T | GRCh38 |
| NC_000016.9:g.2137884C>T , CM000678.1:g.2137884C>T | GRCh37 |
| NC_000016.8:g.2077885C>T | NCBI36 |
| NG_005895.1:g.43578C>T , LRG_487:g.43578C>T | |
| NG_008617.1:g.55338G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3359C>T | ENSP00000455997.2:n.*3359C>T | |
| ENST00000642206.2:c.4857C>T | ENSP00000495146.2:p.His1619= | |
| ENST00000642365.2:c.5007C>T | ENSP00000495459.2:p.His1669= | |
| ENST00000644417.2:c.*5523C>T | ENSP00000493912.2:n.*5523C>T | |
| ENST00000646464.2:c.*7759C>T | ENSP00000496610.2:n.*7759C>T | |
| ENST00000219476.9:c.5010C>T MANE Select | ENSP00000219476.3:p.His1670= | |
| ENST00000350773.9:c.4941C>T | ENSP00000344383.4:p.His1647= | |
| ENST00000401874.7:c.4809C>T | ENSP00000384468.2:p.His1603= | |
| ENST00000568454.6:c.4842C>T | ENSP00000454487.1:p.His1614= | |
| ENST00000569110.2:c.1233C>T | ||
| ENST00000569930.2:n.2892C>T | ||
| ENST00000642365.1:c.3664C>T | ||
| ENST00000642561.1:c.4881C>T | ENSP00000495099.1:p.His1627= | |
| ENST00000642791.1:n.607C>T | ||
| ENST00000642797.1:c.4812C>T | ENSP00000493846.1:p.His1604= | |
| ENST00000642936.1:c.4878C>T | ENSP00000494514.1:p.His1626= | |
| ENST00000643088.1:c.4803C>T | ENSP00000494747.1:p.His1601= | |
| ENST00000643177.1:n.1024C>T | ||
| ENST00000643426.1:n.2658C>T | ||
| ENST00000643946.1:c.4935C>T | ENSP00000495927.1:p.His1645= | |
| ENST00000644043.1:c.4881C>T | ENSP00000496262.1:p.His1627= | |
| ENST00000644278.1:n.492C>T | ||
| ENST00000644329.1:c.4809C>T | ENSP00000496611.1:p.His1603= | |
| ENST00000644335.1:c.4806C>T | ENSP00000496317.1:p.His1602= | |
| ENST00000644399.1:c.4931C>T | ||
| ENST00000645024.1:n.3094C>T | ||
| ENST00000646388.1:c.5004C>T | ENSP00000495921.1:p.His1668= | |
| ENST00000646634.1:n.3825C>T | ||
| ENST00000646674.1:n.2262C>T | ||
| ENST00000647042.1:n.2233C>T | ||
| ENST00000647180.1:n.2123C>T | ||
| ENST00000219476.7:c.5010C>T | ENSP00000219476.3:p.His1670= | |
| ENST00000350773.8:c.4941C>T | ENSP00000344383.4:p.His1647= | |
| ENST00000382538.10:c.4665C>T | ENSP00000371978.6:p.His1555= | |
| ENST00000401874.6:c.4809C>T | ENSP00000384468.2:p.His1603= | |
| ENST00000439117.6:c.*4177C>T | ENSP00000406980.2:n.*4177C>T | |
| ENST00000439673.6:c.4701C>T | ENSP00000399232.2:p.His1567= | |
| ENST00000497886.5:n.2733C>T | ||
| ENST00000568454.5:c.4842C>T | ENSP00000454487.1:p.His1614= | |
| ENST00000569110.1:c.1192C>T | ||
| ENST00000569930.1:n.2125C>T | ||
| NM_000548.3:c.5010C>T , LRG_487t1:c.5010C>T | NP_000539.2:p.His1670= | |
| NM_001077183.1:c.4809C>T | NP_001070651.1:p.His1603= | |
| NM_001114382.1:c.4941C>T | NP_001107854.1:p.His1647= | |
| XM_005255529.3:c.4881C>T | XP_005255586.2:p.His1627= | |
| XM_005255531.3:c.4812C>T | XP_005255588.2:p.His1604= | |
| XM_011522636.1:c.5064C>T | XP_011520938.1:p.His1688= | |
| XM_011522637.1:c.5061C>T | XP_011520939.1:p.His1687= | |
| XM_011522638.1:c.4953C>T | XP_011520940.1:p.His1651= | |
| XM_011522639.1:c.4935C>T | XP_011520941.1:p.His1645= | |
| XM_011522640.1:c.4932C>T | XP_011520942.1:p.His1644= | |
| XM_011522641.1:c.4701C>T | XP_011520943.1:p.His1567= | |
| NM_000548.4:c.5010C>T | NP_000539.2:p.His1670= | |
| NM_001077183.2:c.4809C>T | NP_001070651.1:p.His1603= | |
| NM_001114382.2:c.4941C>T | NP_001107854.1:p.His1647= | |
| NM_001318827.1:c.4701C>T | NP_001305756.1:p.His1567= | |
| NM_001318829.1:c.4665C>T | NP_001305758.1:p.His1555= | |
| NM_001318831.1:c.4278C>T | NP_001305760.1:p.His1426= | |
| NM_001318832.1:c.4842C>T | NP_001305761.1:p.His1614= | |
| NM_001363528.1:c.4812C>T | NP_001350457.1:p.His1604= | |
| NM_021055.2:c.4881C>T | NP_066399.2:p.His1627= | |
| XM_005255531.4:c.4812C>T | XP_005255588.2:p.His1604= | |
| XM_011522636.2:c.5064C>T | XP_011520938.1:p.His1688= | |
| XM_011522637.2:c.5061C>T | XP_011520939.1:p.His1687= | |
| XM_011522638.2:c.5226C>T | XP_011520940.2:p.His1742= | |
| XM_011522639.2:c.4935C>T | XP_011520941.1:p.His1645= | |
| XM_011522640.2:c.4932C>T | XP_011520942.1:p.His1644= | |
| XM_017023615.1:c.5007C>T | XP_016879104.1:p.His1669= | |
| XM_017023616.1:c.4878C>T | XP_016879105.1:p.His1626= | |
| XM_017023617.1:c.4974C>T | XP_016879106.1:p.His1658= | |
| XM_017023618.1:c.3720C>T | XP_016879107.1:p.His1240= | |
| XM_024450413.1:c.4809C>T | XP_024306181.1:p.His1603= | |
| NM_000548.5:c.5010C>T MANE Select | NP_000539.2:p.His1670= | |
| NM_001370404.1:c.4878C>T | NP_001357333.1:p.His1626= | |
| NM_001370405.1:c.4881C>T | NP_001357334.1:p.His1627= | |
| NM_001077183.3:c.4809C>T | NP_001070651.1:p.His1603= | |
| NM_001114382.3:c.4941C>T | NP_001107854.1:p.His1647= | |
| NM_001318827.2:c.4701C>T | NP_001305756.1:p.His1567= | |
| NM_001318829.2:c.4665C>T | NP_001305758.1:p.His1555= | |
| NM_001318831.2:c.4278C>T | NP_001305760.1:p.His1426= | |
| NM_001318832.2:c.4842C>T | NP_001305761.1:p.His1614= | |
| NM_001363528.2:c.4812C>T | NP_001350457.1:p.His1604= | |
| NM_021055.3:c.4881C>T | NP_066399.2:p.His1627= |