Linked Data
dbSNP Id:
rs755616853
ExAC:
2:157182672 A / C
gnomAD v2:
2-157182672-A-C
gnomAD v3:
2-156326160-A-C
gnomAD v4:
2-156326160-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.156326160A>C , CM000664.2:g.156326160A>C | GRCh38 |
| NC_000002.11:g.157182672A>C , CM000664.1:g.157182672A>C | GRCh37 |
| NC_000002.10:g.156890918A>C | NCBI36 |
| NG_011821.1:g.11616T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700228.1:c.1326T>G | ENSP00000514865.1:p.Ala442= | |
| ENST00000700229.1:c.494T>G | ||
| ENST00000700230.1:c.1070T>G | ENSP00000514867.1:n.1070T>G | |
| ENST00000700231.1:c.1455T>G | ENSP00000514868.1:p.Ala485= | |
| ENST00000339562.9:c.1530T>G MANE Select | ENSP00000344479.4:p.Ala510= | |
| ENST00000675870.1:c.*41T>G | ENSP00000502739.1:n.*41T>G | |
| ENST00000339562.8:c.1530T>G | ENSP00000344479.4:p.Ala510= | |
| ENST00000409108.6:c.1426T>G | ENSP00000386993.2:p.Tyr476Asp | |
| ENST00000409572.5:c.1530T>G | ENSP00000386747.1:p.Ala510= | |
| ENST00000417764.5:c.*41T>G | ENSP00000415632.1:n.*41T>G | |
| ENST00000417972.5:c.*41T>G | ENSP00000394671.1:n.*41T>G | |
| ENST00000426264.5:c.1341T>G | ENSP00000389986.1:p.Ala447= | |
| ENST00000429376.5:c.1237T>G | ENSP00000410952.1:p.Tyr413Asp | |
| NM_006186.3:c.1530T>G | NP_006177.1:p.Ala510= | |
| XM_005246621.2:c.1563T>G | XP_005246678.1:p.Ala521= | |
| XM_005246622.2:c.1341T>G | XP_005246679.1:p.Ala447= | |
| XM_005246623.1:c.1341T>G | XP_005246680.1:p.Ala447= | |
| XM_006712553.2:c.1488T>G | XP_006712616.1:p.Ala496= | |
| XM_011511246.1:c.1459T>G | XP_011509548.1:p.Tyr487Asp | |
| XR_427087.2:n.3615T>G | ||
| NM_173173.2:c.1341T>G | NP_775265.1:p.Ala447= | |
| XM_005246621.4:c.1563T>G | XP_005246678.1:p.Ala521= | |
| XM_006712553.4:c.1488T>G | XP_006712616.1:p.Ala496= | |
| XM_011511246.2:c.1459T>G | XP_011509548.1:p.Tyr487Asp | |
| XM_017004219.2:c.1530T>G | XP_016859708.1:p.Ala510= | |
| XM_017004220.2:c.1455T>G | XP_016859709.1:p.Ala485= | |
| XR_001738751.2:n.1777T>G | ||
| XR_001738752.2:n.1599T>G | ||
| XR_427087.4:n.1656T>G | ||
| NM_006186.4:c.1530T>G MANE Select | NP_006177.1:p.Ala510= | |
| NM_173173.3:c.1341T>G | NP_775265.1:p.Ala447= |