Linked Data
ClinVar Variation Id:
317049
dbSNP Id:
rs766510036
ExAC:
15:72668317 C / T
gnomAD v2:
15-72668317-C-T
gnomAD v3:
15-72375976-C-T
gnomAD v4:
15-72375976-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72375976C>T , CM000677.2:g.72375976C>T | GRCh38 |
| NC_000015.9:g.72668317C>T , CM000677.1:g.72668317C>T | GRCh37 |
| NC_000015.8:g.70455371C>T | NCBI36 |
| NG_009017.1:g.5204G>A | |
| NG_009017.2:g.5204G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563908.2:n.10G>A | ||
| ENST00000567027.6:c.-4G>A | ENSP00000457521.2:n.-4G>A | |
| ENST00000682061.1:c.-4G>A | ENSP00000508316.1:n.-4G>A | |
| ENST00000682653.1:n.28G>A | ||
| ENST00000682657.1:c.-4G>A | ENSP00000507753.1:n.-4G>A | |
| ENST00000682721.1:c.-4G>A | ENSP00000507535.1:n.-4G>A | |
| ENST00000682843.1:c.-4G>A | ENSP00000508173.1:n.-4G>A | |
| ENST00000683003.1:c.-4G>A | ENSP00000507576.1:n.-4G>A | |
| ENST00000683228.1:n.28G>A | ||
| ENST00000683243.1:c.-4G>A | ENSP00000507042.1:n.-4G>A | |
| ENST00000683463.1:c.-4G>A | ENSP00000507986.1:n.-4G>A | |
| ENST00000683548.1:n.28G>A | ||
| ENST00000683579.1:c.-4G>A | ENSP00000506867.1:n.-4G>A | |
| ENST00000683587.1:n.28G>A | ||
| ENST00000683681.1:c.-4G>A | ENSP00000508110.1:n.-4G>A | |
| ENST00000683735.1:c.-4G>A | ENSP00000508336.1:n.-4G>A | |
| ENST00000683853.1:c.-4G>A | ENSP00000506834.1:n.-4G>A | |
| ENST00000683860.1:c.-4G>A | ENSP00000507179.1:n.-4G>A | |
| ENST00000683884.1:c.-4G>A | ENSP00000507004.1:n.-4G>A | |
| ENST00000684041.1:c.-4G>A | ENSP00000508382.1:n.-4G>A | |
| ENST00000684125.1:c.-4G>A | ENSP00000507320.1:n.-4G>A | |
| ENST00000684203.1:n.14G>A | ||
| ENST00000684231.1:c.-4G>A | ENSP00000507748.1:n.-4G>A | |
| ENST00000684263.1:c.-4G>A | ENSP00000508369.1:n.-4G>A | |
| ENST00000684415.1:c.-4G>A | ENSP00000507227.1:n.-4G>A | |
| ENST00000684520.1:c.-4G>A | ENSP00000506826.1:n.-4G>A | |
| ENST00000684602.1:c.-4G>A | ENSP00000507996.1:n.-4G>A | |
| ENST00000268097.10:c.-4G>A MANE Select | ENSP00000268097.6:n.-4G>A | |
| ENST00000268097.9:c.-4G>A | ENSP00000268097.5:n.-4G>A | |
| ENST00000379915.4:c.-4G>A | ENSP00000478716.1:n.-4G>A | |
| ENST00000566304.5:c.-4G>A | ENSP00000455114.1:n.-4G>A | |
| ENST00000566672.5:c.-4G>A | ENSP00000457037.1:n.-4G>A | |
| ENST00000567159.5:c.-4G>A | ENSP00000456489.1:n.-4G>A | |
| ENST00000567213.2:c.-4G>A | ENSP00000478217.1:n.-4G>A | |
| ENST00000567411.5:c.-4G>A | ENSP00000455545.1:n.-4G>A | |
| ENST00000569509.5:n.147-145G>A | ||
| NM_000520.4:c.-4G>A | NP_000511.2:n.-4G>A | |
| NM_000520.5:c.-4G>A | NP_000511.2:n.-4G>A | |
| NM_001318825.1:c.-4G>A | NP_001305754.1:n.-4G>A | |
| NR_134869.1:n.498G>A | ||
| NM_000520.6:c.-4G>A MANE Select | NP_000511.2:n.-4G>A | |
| NM_001318825.2:c.-4G>A | NP_001305754.1:n.-4G>A | |
| NR_134869.2:n.39G>A | ||
| NR_134869.3:n.39G>A |