Linked Data
dbSNP Id:
rs752278607
ExAC:
2:157182671 T / C
gnomAD v2:
2-157182671-T-C
gnomAD v3:
2-156326159-T-C
gnomAD v4:
2-156326159-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.156326159T>C , CM000664.2:g.156326159T>C | GRCh38 |
| NC_000002.11:g.157182671T>C , CM000664.1:g.157182671T>C | GRCh37 |
| NC_000002.10:g.156890917T>C | NCBI36 |
| NG_011821.1:g.11617A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700228.1:c.1327A>G | ENSP00000514865.1:p.Met443Val | |
| ENST00000700229.1:c.495A>G | ||
| ENST00000700230.1:c.1071A>G | ENSP00000514867.1:n.1071A>G | |
| ENST00000700231.1:c.1456A>G | ENSP00000514868.1:p.Met486Val | |
| ENST00000339562.9:c.1531A>G MANE Select | ENSP00000344479.4:p.Met511Val | |
| ENST00000675870.1:c.*42A>G | ENSP00000502739.1:n.*42A>G | |
| ENST00000339562.8:c.1531A>G | ENSP00000344479.4:p.Met511Val | |
| ENST00000409108.6:c.1427A>G | ENSP00000386993.2:p.Tyr476Cys | |
| ENST00000409572.5:c.1531A>G | ENSP00000386747.1:p.Met511Val | |
| ENST00000417764.5:c.*42A>G | ENSP00000415632.1:n.*42A>G | |
| ENST00000417972.5:c.*42A>G | ENSP00000394671.1:n.*42A>G | |
| ENST00000426264.5:c.1342A>G | ENSP00000389986.1:p.Met448Val | |
| ENST00000429376.5:c.1238A>G | ENSP00000410952.1:p.Tyr413Cys | |
| NM_006186.3:c.1531A>G | NP_006177.1:p.Met511Val | |
| XM_005246621.2:c.1564A>G | XP_005246678.1:p.Met522Val | |
| XM_005246622.2:c.1342A>G | XP_005246679.1:p.Met448Val | |
| XM_005246623.1:c.1342A>G | XP_005246680.1:p.Met448Val | |
| XM_006712553.2:c.1489A>G | XP_006712616.1:p.Met497Val | |
| XM_011511246.1:c.1460A>G | XP_011509548.1:p.Tyr487Cys | |
| XR_427087.2:n.3616A>G | ||
| NM_173173.2:c.1342A>G | NP_775265.1:p.Met448Val | |
| XM_005246621.4:c.1564A>G | XP_005246678.1:p.Met522Val | |
| XM_006712553.4:c.1489A>G | XP_006712616.1:p.Met497Val | |
| XM_011511246.2:c.1460A>G | XP_011509548.1:p.Tyr487Cys | |
| XM_017004219.2:c.1531A>G | XP_016859708.1:p.Met511Val | |
| XM_017004220.2:c.1456A>G | XP_016859709.1:p.Met486Val | |
| XR_001738751.2:n.1778A>G | ||
| XR_001738752.2:n.1600A>G | ||
| XR_427087.4:n.1657A>G | ||
| NM_006186.4:c.1531A>G MANE Select | NP_006177.1:p.Met511Val | |
| NM_173173.3:c.1342A>G | NP_775265.1:p.Met448Val |