Linked Data
ClinVar Variation Id:
1982939
dbSNP Id:
rs777212186
ExAC:
15:72639033 T / C
gnomAD v2:
15-72639033-T-C
gnomAD v3:
15-72346692-T-C
gnomAD v4:
15-72346692-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72346692T>C , CM000677.2:g.72346692T>C | GRCh38 |
| NC_000015.9:g.72639033T>C , CM000677.1:g.72639033T>C | GRCh37 |
| NC_000015.8:g.70426087T>C | NCBI36 |
| NG_009017.1:g.34488A>G | |
| NG_009017.2:g.34488A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.1074-367A>G | ENSP00000457521.2:n.1074-367A>G | |
| ENST00000682061.1:c.*827A>G | ENSP00000508316.1:n.*827A>G | |
| ENST00000682064.1:n.507A>G | ||
| ENST00000682177.1:c.1208A>G | ENSP00000507409.1:n.1208A>G | |
| ENST00000682235.1:n.504A>G | ||
| ENST00000682461.1:c.1271A>G | ENSP00000507308.1:n.1271A>G | |
| ENST00000682653.1:n.1485A>G | ||
| ENST00000682657.1:c.*484-367A>G | ENSP00000507753.1:n.*484-367A>G | |
| ENST00000682721.1:c.*968A>G | ENSP00000507535.1:n.*968A>G | |
| ENST00000682843.1:c.*972-367A>G | ENSP00000508173.1:n.*972-367A>G | |
| ENST00000683003.1:c.*484-367A>G | ENSP00000507576.1:n.*484-367A>G | |
| ENST00000683133.1:c.1349A>G | ENSP00000508108.1:n.1349A>G | |
| ENST00000683243.1:c.*484-367A>G | ENSP00000507042.1:n.*484-367A>G | |
| ENST00000683463.1:c.1092A>G | ENSP00000507986.1:p.Ser364= | |
| ENST00000683548.1:n.1105-367A>G | ||
| ENST00000683579.1:c.*1063A>G | ENSP00000506867.1:n.*1063A>G | |
| ENST00000683587.1:n.1178-367A>G | ||
| ENST00000683681.1:c.1165A>G | ENSP00000508110.1:p.Ile389Val | |
| ENST00000683735.1:c.*1045-367A>G | ENSP00000508336.1:n.*1045-367A>G | |
| ENST00000683853.1:c.1092A>G | ENSP00000506834.1:p.Ser364= | |
| ENST00000683860.1:c.1165A>G | ENSP00000507179.1:p.Ile389Val | |
| ENST00000683884.1:c.1147-367A>G | ENSP00000507004.1:n.1147-367A>G | |
| ENST00000684041.1:c.1165A>G | ENSP00000508382.1:p.Ile389Val | |
| ENST00000684125.1:c.1074-367A>G | ENSP00000507320.1:n.1074-367A>G | |
| ENST00000684203.1:n.2930A>G | ||
| ENST00000684231.1:c.*575A>G | ENSP00000507748.1:n.*575A>G | |
| ENST00000684263.1:c.*105A>G | ENSP00000508369.1:n.*105A>G | |
| ENST00000684305.1:c.1613A>G | ENSP00000506819.1:n.1613A>G | |
| ENST00000684415.1:c.*32A>G | ENSP00000507227.1:n.*32A>G | |
| ENST00000684520.1:c.1165A>G | ENSP00000506826.1:p.Ile389Val | |
| ENST00000684602.1:c.*831A>G | ENSP00000507996.1:n.*831A>G | |
| ENST00000684667.1:c.1496A>G | ENSP00000507003.1:n.1496A>G | |
| ENST00000268097.10:c.1165A>G MANE Select | ENSP00000268097.6:p.Ile389Val | |
| ENST00000268097.9:c.1165A>G | ENSP00000268097.5:p.Ile389Val | |
| ENST00000379915.4:c.413-367A>G | ENSP00000478716.1:n.413-367A>G | |
| ENST00000563762.5:c.826-367A>G | ENSP00000456346.1:n.826-367A>G | |
| ENST00000566304.5:c.1198A>G | ENSP00000455114.1:p.Ile400Val | |
| ENST00000566672.5:c.*575A>G | ENSP00000457037.1:n.*575A>G | |
| ENST00000567027.5:c.946-367A>G | ||
| ENST00000567159.5:c.1165A>G | ENSP00000456489.1:p.Ile389Val | |
| ENST00000567411.5:c.*686A>G | ENSP00000455545.1:n.*686A>G | |
| ENST00000568777.5:n.6551-367A>G | ||
| ENST00000569410.5:c.1092A>G | ENSP00000457125.1:p.Ser364= | |
| NM_000520.4:c.1165A>G | NP_000511.2:p.Ile389Val | |
| NM_000520.5:c.1165A>G | NP_000511.2:p.Ile389Val | |
| NM_001318825.1:c.1198A>G | NP_001305754.1:p.Ile400Val | |
| NR_134869.1:n.1575-367A>G | ||
| NM_000520.6:c.1165A>G MANE Select | NP_000511.2:p.Ile389Val | |
| NM_001318825.2:c.1198A>G | NP_001305754.1:p.Ile400Val | |
| NR_134869.2:n.1116-367A>G | ||
| NR_134869.3:n.1116-367A>G |