Linked Data
ClinVar Variation Id:
2069681
dbSNP Id:
rs759434633
ExAC:
15:72640059 C / A
gnomAD v2:
15-72640059-C-A
gnomAD v3:
15-72347718-C-A
gnomAD v4:
15-72347718-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72347718C>A , CM000677.2:g.72347718C>A | GRCh38 |
| NC_000015.9:g.72640059C>A , CM000677.1:g.72640059C>A | GRCh37 |
| NC_000015.8:g.70427113C>A | NCBI36 |
| NG_009017.1:g.33462G>T | |
| NG_009017.2:g.33462G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.1073+330G>T | ENSP00000457521.2:n.1073+330G>T | |
| ENST00000682061.1:c.*776G>T | ENSP00000508316.1:n.*776G>T | |
| ENST00000682177.1:c.1157G>T | ENSP00000507409.1:n.1157G>T | |
| ENST00000682461.1:c.1220G>T | ENSP00000507308.1:n.1220G>T | |
| ENST00000682653.1:n.1434G>T | ||
| ENST00000682657.1:c.*483+330G>T | ENSP00000507753.1:n.*483+330G>T | |
| ENST00000682721.1:c.*917G>T | ENSP00000507535.1:n.*917G>T | |
| ENST00000682843.1:c.*971+330G>T | ENSP00000508173.1:n.*971+330G>T | |
| ENST00000683003.1:c.*483+330G>T | ENSP00000507576.1:n.*483+330G>T | |
| ENST00000683133.1:c.1298G>T | ENSP00000508108.1:n.1298G>T | |
| ENST00000683228.1:n.1145G>T | ||
| ENST00000683243.1:c.*483+330G>T | ENSP00000507042.1:n.*483+330G>T | |
| ENST00000683463.1:c.1073+330G>T | ENSP00000507986.1:n.1073+330G>T | |
| ENST00000683548.1:n.1104+330G>T | ||
| ENST00000683579.1:c.*1012G>T | ENSP00000506867.1:n.*1012G>T | |
| ENST00000683587.1:n.1145G>T | ||
| ENST00000683681.1:c.1114G>T | ENSP00000508110.1:p.Val372Leu | |
| ENST00000683735.1:c.*1012G>T | ENSP00000508336.1:n.*1012G>T | |
| ENST00000683742.1:n.945G>T | ||
| ENST00000683853.1:c.1073+330G>T | ENSP00000506834.1:n.1073+330G>T | |
| ENST00000683860.1:c.1114G>T | ENSP00000507179.1:p.Val372Leu | |
| ENST00000683884.1:c.1114G>T | ENSP00000507004.1:p.Val372Leu | |
| ENST00000684041.1:c.1114G>T | ENSP00000508382.1:p.Val372Leu | |
| ENST00000684125.1:c.1073+330G>T | ENSP00000507320.1:n.1073+330G>T | |
| ENST00000684203.1:n.2911+330G>T | ||
| ENST00000684231.1:c.*524G>T | ENSP00000507748.1:n.*524G>T | |
| ENST00000684263.1:c.*54G>T | ENSP00000508369.1:n.*54G>T | |
| ENST00000684305.1:c.1562G>T | ENSP00000506819.1:n.1562G>T | |
| ENST00000684415.1:c.*13+313G>T | ENSP00000507227.1:n.*13+313G>T | |
| ENST00000684520.1:c.1114G>T | ENSP00000506826.1:p.Val372Leu | |
| ENST00000684602.1:c.*780G>T | ENSP00000507996.1:n.*780G>T | |
| ENST00000684667.1:c.1445G>T | ENSP00000507003.1:n.1445G>T | |
| ENST00000268097.10:c.1114G>T MANE Select | ENSP00000268097.6:p.Val372Leu | |
| ENST00000268097.9:c.1114G>T | ENSP00000268097.5:p.Val372Leu | |
| ENST00000379915.4:c.413-1393G>T | ENSP00000478716.1:n.413-1393G>T | |
| ENST00000563762.5:c.825+330G>T | ENSP00000456346.1:n.825+330G>T | |
| ENST00000566304.5:c.1147G>T | ENSP00000455114.1:p.Val383Leu | |
| ENST00000566672.5:c.*524G>T | ENSP00000457037.1:n.*524G>T | |
| ENST00000567027.5:c.945+330G>T | ||
| ENST00000567159.5:c.1114G>T | ENSP00000456489.1:p.Val372Leu | |
| ENST00000567411.5:c.*635G>T | ENSP00000455545.1:n.*635G>T | |
| ENST00000568777.5:n.6518G>T | ||
| ENST00000569410.5:c.1073+330G>T | ENSP00000457125.1:n.1073+330G>T | |
| NM_000520.4:c.1114G>T | NP_000511.2:p.Val372Leu | |
| NM_000520.5:c.1114G>T | NP_000511.2:p.Val372Leu | |
| NM_001318825.1:c.1147G>T | NP_001305754.1:p.Val383Leu | |
| NR_134869.1:n.1574+330G>T | ||
| NM_000520.6:c.1114G>T MANE Select | NP_000511.2:p.Val372Leu | |
| NM_001318825.2:c.1147G>T | NP_001305754.1:p.Val383Leu | |
| NR_134869.2:n.1115+330G>T | ||
| NR_134869.3:n.1115+330G>T |