Linked Data
ClinVar Variation Id:
403668
dbSNP Id:
rs372617572
ExAC:
X:76938598 G / A
gnomAD v2:
X-76938598-G-A
gnomAD v3:
X-77683106-G-A
gnomAD v4:
X-77683106-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.77683106G>A , CM000685.2:g.77683106G>A | GRCh38 |
| NC_000023.10:g.76938598G>A , CM000685.1:g.76938598G>A | GRCh37 |
| NC_000023.9:g.76825254G>A | NCBI36 |
| NG_008838.2:g.108116C>T | |
| NG_008838.3:g.108164C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373344.11:c.2150C>T MANE Select | ENSP00000362441.4:p.Pro717Leu | |
| ENST00000373344.9:c.2150C>T | ENSP00000362441.4:p.Pro717Leu | |
| ENST00000395603.7:c.2036C>T | ENSP00000378967.3:p.Pro679Leu | |
| ENST00000480283.5:c.*1778C>T | ENSP00000480196.1:n.*1778C>T | |
| ENST00000624032.3:c.2063C>T | ENSP00000485253.1:p.Pro688Leu | |
| ENST00000624166.3:c.1946C>T | ENSP00000485103.1:p.Pro649Leu | |
| NM_000489.4:c.2150C>T | NP_000480.3:p.Pro717Leu | |
| NM_138270.3:c.2036C>T | NP_612114.2:p.Pro679Leu | |
| XM_005262153.3:c.2147C>T | XP_005262210.2:p.Pro716Leu | |
| XM_005262154.3:c.2063C>T | XP_005262211.2:p.Pro688Leu | |
| XM_005262155.3:c.2033C>T | XP_005262212.2:p.Pro678Leu | |
| XM_005262156.3:c.1985C>T | XP_005262213.2:p.Pro662Leu | |
| XM_005262157.3:c.1946C>T | XP_005262214.2:p.Pro649Leu | |
| XM_006724666.2:c.2033C>T | XP_006724729.1:p.Pro678Leu | |
| XM_006724667.2:c.1871C>T | XP_006724730.1:p.Pro624Leu | |
| XM_006724668.2:c.2150C>T | XP_006724731.1:p.Pro717Leu | |
| XR_938400.1:n.2418C>T | ||
| NM_000489.5:c.2150C>T | NP_000480.3:p.Pro717Leu | |
| XM_005262153.5:c.2147C>T | XP_005262210.2:p.Pro716Leu | |
| XM_005262154.5:c.2063C>T | XP_005262211.2:p.Pro688Leu | |
| XM_005262155.4:c.2033C>T | XP_005262212.2:p.Pro678Leu | |
| XM_005262156.4:c.1985C>T | XP_005262213.2:p.Pro662Leu | |
| XM_005262157.5:c.1946C>T | XP_005262214.2:p.Pro649Leu | |
| XM_006724666.4:c.2033C>T | XP_006724729.1:p.Pro678Leu | |
| XM_006724667.3:c.1871C>T | XP_006724730.1:p.Pro624Leu | |
| XM_006724668.3:c.2150C>T | XP_006724731.1:p.Pro717Leu | |
| XM_017029601.2:c.2060C>T | XP_016885090.1:p.Pro687Leu | |
| XM_017029602.1:c.2030C>T | XP_016885091.1:p.Pro677Leu | |
| XM_017029603.1:c.1982C>T | XP_016885092.1:p.Pro661Leu | |
| XM_017029604.2:c.1949C>T | XP_016885093.1:p.Pro650Leu | |
| XM_017029605.1:c.1946C>T | XP_016885094.1:p.Pro649Leu | |
| XM_017029606.2:c.1919C>T | XP_016885095.1:p.Pro640Leu | |
| XM_017029607.2:c.1916C>T | XP_016885096.1:p.Pro639Leu | |
| XM_017029608.2:c.1868C>T | XP_016885097.1:p.Pro623Leu | |
| XM_017029609.1:c.1832C>T | XP_016885098.1:p.Pro611Leu | |
| XM_017029610.1:c.1829C>T | XP_016885099.1:p.Pro610Leu | |
| XM_017029611.1:c.1784C>T | XP_016885100.1:p.Pro595Leu | |
| XR_001755700.2:n.2375C>T | ||
| NM_138270.4:c.2036C>T | NP_612114.2:p.Pro679Leu | |
| NM_000489.6:c.2150C>T MANE Select | NP_000480.3:p.Pro717Leu | |
| NM_138270.5:c.2036C>T | NP_612114.2:p.Pro679Leu |