Linked Data
ClinVar Variation Id:
310423
dbSNP Id:
rs376649488
ExAC:
12:7356090 T / C
gnomAD v2:
12-7356090-T-C
gnomAD v3:
12-7203494-T-C
gnomAD v4:
12-7203494-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7203494T>C , CM000674.2:g.7203494T>C | GRCh38 |
| NC_000012.11:g.7356090T>C , CM000674.1:g.7356090T>C | GRCh37 |
| NC_000012.10:g.7247357T>C | NCBI36 |
| NG_008448.1:g.19332T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675855.1:c.909T>C MANE Select | ENSP00000502374.1:p.Ala303= | |
| ENST00000266563.9:c.798T>C | ENSP00000266563.5:p.Ala266= | |
| ENST00000266564.7:c.885T>C | ENSP00000266564.3:p.Ala295= | |
| ENST00000396637.7:c.819T>C | ENSP00000379877.3:p.Ala273= | |
| ENST00000412720.6:c.972T>C | ENSP00000391601.2:p.Ala324= | |
| ENST00000420616.6:c.909T>C | ENSP00000410159.2:p.Ala303= | |
| ENST00000434354.6:c.954T>C | ENSP00000407401.2:p.Ala318= | |
| ENST00000455147.6:c.909T>C | ENSP00000400647.2:p.Ala303= | |
| ENST00000545574.5:c.762T>C | ENSP00000443500.1:p.Ala254= | |
| NM_000319.4:c.885T>C | NP_000310.2:p.Ala295= | |
| NM_001131023.1:c.954T>C | NP_001124495.1:p.Ala318= | |
| NM_001131024.1:c.798T>C | NP_001124496.1:p.Ala266= | |
| NM_001131025.1:c.909T>C | NP_001124497.1:p.Ala303= | |
| NM_001131026.1:c.909T>C | NP_001124498.1:p.Ala303= | |
| NM_001300789.1:c.972T>C | NP_001287718.1:p.Ala324= | |
| XM_005253455.1:c.861T>C | XP_005253512.1:p.Ala287= | |
| XM_011520793.1:c.1017T>C | XP_011519095.1:p.Ala339= | |
| XM_011520794.1:c.1017T>C | XP_011519096.1:p.Ala339= | |
| XM_011520795.1:c.954T>C | XP_011519097.1:p.Ala318= | |
| XM_011520796.1:c.954T>C | XP_011519098.1:p.Ala318= | |
| XM_011520797.1:c.909T>C | XP_011519099.1:p.Ala303= | |
| XM_011520798.1:c.909T>C | XP_011519100.1:p.Ala303= | |
| XM_011520799.1:c.909T>C | XP_011519101.1:p.Ala303= | |
| XM_011520800.1:c.909T>C | XP_011519102.1:p.Ala303= | |
| XM_011520801.1:c.906T>C | XP_011519103.1:p.Ala302= | |
| XM_011520802.1:c.660T>C | XP_011519104.1:p.Ala220= | |
| NM_001351124.1:c.798T>C | NP_001338053.1:p.Ala266= | |
| NM_001351126.1:c.798T>C | NP_001338055.1:p.Ala266= | |
| NM_001351127.1:c.798T>C | NP_001338056.1:p.Ala266= | |
| NM_001351128.1:c.798T>C | NP_001338057.1:p.Ala266= | |
| NM_001351130.1:c.798T>C | NP_001338059.1:p.Ala266= | |
| NM_001351131.1:c.909T>C | NP_001338060.1:p.Ala303= | |
| NM_001351132.1:c.909T>C | NP_001338061.1:p.Ala303= | |
| NM_001351133.1:c.909T>C | NP_001338062.1:p.Ala303= | |
| NM_001351134.1:c.909T>C | NP_001338063.1:p.Ala303= | |
| NM_001351135.1:c.906T>C | NP_001338064.1:p.Ala302= | |
| NM_001351136.1:c.909T>C | NP_001338065.1:p.Ala303= | |
| NM_001351137.1:c.861T>C | NP_001338066.1:p.Ala287= | |
| NM_001351138.1:c.843T>C | NP_001338067.1:p.Ala281= | |
| NM_001351139.1:c.774T>C | NP_001338068.1:p.Ala258= | |
| NM_001351140.1:c.774T>C | NP_001338069.1:p.Ala258= | |
| XM_011520793.2:c.1017T>C | XP_011519095.1:p.Ala339= | |
| XM_011520802.2:c.660T>C | XP_011519104.1:p.Ala220= | |
| XM_017019744.1:c.1353T>C | XP_016875233.1:p.Ala451= | |
| XM_017019745.1:c.1353T>C | XP_016875234.1:p.Ala451= | |
| XM_017019746.1:c.1242T>C | XP_016875235.1:p.Ala414= | |
| XM_017019747.1:c.1218T>C | XP_016875236.1:p.Ala406= | |
| XM_017019748.1:c.954T>C | XP_016875237.1:p.Ala318= | |
| XM_017019749.1:c.909T>C | XP_016875238.1:p.Ala303= | |
| XM_017019750.1:c.885T>C | XP_016875239.1:p.Ala295= | |
| XR_001748833.1:n.1395T>C | ||
| NM_000319.5:c.885T>C | NP_000310.2:p.Ala295= | |
| NM_001131023.2:c.954T>C | NP_001124495.1:p.Ala318= | |
| NM_001131024.2:c.798T>C | NP_001124496.1:p.Ala266= | |
| NM_001131025.2:c.909T>C | NP_001124497.1:p.Ala303= | |
| NM_001131026.2:c.909T>C | NP_001124498.1:p.Ala303= | |
| NM_001300789.3:c.909T>C | NP_001287718.2:p.Ala303= | |
| NM_001351124.3:c.798T>C | NP_001338053.1:p.Ala266= | |
| NM_001351126.2:c.798T>C | NP_001338055.1:p.Ala266= | |
| NM_001351127.2:c.798T>C | NP_001338056.1:p.Ala266= | |
| NM_001351128.2:c.798T>C | NP_001338057.1:p.Ala266= | |
| NM_001351130.3:c.798T>C | NP_001338059.1:p.Ala266= | |
| NM_001351131.2:c.909T>C | NP_001338060.1:p.Ala303= | |
| NM_001351132.2:c.909T>C MANE Select | NP_001338061.1:p.Ala303= | |
| NM_001351133.2:c.909T>C | NP_001338062.1:p.Ala303= | |
| NM_001351134.2:c.909T>C | NP_001338063.1:p.Ala303= | |
| NM_001351135.3:c.843T>C | NP_001338064.2:p.Ala281= | |
| NM_001351136.2:c.909T>C | NP_001338065.1:p.Ala303= | |
| NM_001351137.3:c.798T>C | NP_001338066.2:p.Ala266= | |
| NM_001351138.2:c.843T>C | NP_001338067.1:p.Ala281= | |
| NM_001351139.2:c.774T>C | NP_001338068.1:p.Ala258= | |
| NM_001351140.2:c.774T>C | NP_001338069.1:p.Ala258= | |
| NM_001374645.1:c.798T>C | NP_001361574.1:p.Ala266= | |
| NM_001374646.1:c.798T>C | NP_001361575.1:p.Ala266= | |
| NM_001374647.2:c.909T>C | NP_001361576.1:p.Ala303= | |
| NM_001374648.2:c.798T>C | NP_001361577.1:p.Ala266= | |
| NM_001374649.2:c.774T>C | NP_001361578.1:p.Ala258= |