Linked Data
ClinVar Variation Id:
555956
ClinVar RCV Id:
RCV000671879
dbSNP Id:
rs121907955
ExAC:
15:72637802 C / A
gnomAD v2:
15-72637802-C-A
gnomAD v4:
15-72345461-C-A
COSMIC:
COSM254720
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72345461C>A , CM000677.2:g.72345461C>A | GRCh38 |
| NC_000015.9:g.72637802C>A , CM000677.1:g.72637802C>A | GRCh37 |
| NC_000015.8:g.70424856C>A | NCBI36 |
| NG_009017.1:g.35719G>T | |
| NG_009017.2:g.35719G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.*171G>T | ENSP00000457521.2:n.*171G>T | |
| ENST00000682061.1:c.*1857G>T | ENSP00000508316.1:n.*1857G>T | |
| ENST00000682064.1:n.1738G>T | ||
| ENST00000682177.1:c.1554G>T | ENSP00000507409.1:n.1554G>T | |
| ENST00000682235.1:n.1534G>T | ||
| ENST00000682461.1:c.1617G>T | ENSP00000507308.1:n.1617G>T | |
| ENST00000682653.1:n.2515G>T | ||
| ENST00000682657.1:c.*1348G>T | ENSP00000507753.1:n.*1348G>T | |
| ENST00000682721.1:c.*1314G>T | ENSP00000507535.1:n.*1314G>T | |
| ENST00000682843.1:c.*1152G>T | ENSP00000508173.1:n.*1152G>T | |
| ENST00000683003.1:c.*1348G>T | ENSP00000507576.1:n.*1348G>T | |
| ENST00000683133.1:c.1695G>T | ENSP00000508108.1:n.1695G>T | |
| ENST00000683243.1:c.*664G>T | ENSP00000507042.1:n.*664G>T | |
| ENST00000683463.1:c.*1000G>T | ENSP00000507986.1:n.*1000G>T | |
| ENST00000683548.1:n.1969G>T | ||
| ENST00000683579.1:c.*1409G>T | ENSP00000506867.1:n.*1409G>T | |
| ENST00000683587.1:n.2042G>T | ||
| ENST00000683681.1:c.*189G>T | ENSP00000508110.1:n.*189G>T | |
| ENST00000683735.1:c.*1909G>T | ENSP00000508336.1:n.*1909G>T | |
| ENST00000683853.1:c.*316G>T | ENSP00000506834.1:n.*316G>T | |
| ENST00000683860.1:c.*631G>T | ENSP00000507179.1:n.*631G>T | |
| ENST00000683884.1:c.*838G>T | ENSP00000507004.1:n.*838G>T | |
| ENST00000684125.1:c.*171G>T | ENSP00000507320.1:n.*171G>T | |
| ENST00000684203.1:n.3960G>T | ||
| ENST00000684231.1:c.*921G>T | ENSP00000507748.1:n.*921G>T | |
| ENST00000684263.1:c.*1135G>T | ENSP00000508369.1:n.*1135G>T | |
| ENST00000684305.1:c.1959G>T | ENSP00000506819.1:n.1959G>T | |
| ENST00000684415.1:c.*1062G>T | ENSP00000507227.1:n.*1062G>T | |
| ENST00000684520.1:c.*770G>T | ENSP00000506826.1:n.*770G>T | |
| ENST00000684602.1:c.*1177G>T | ENSP00000507996.1:n.*1177G>T | |
| ENST00000684667.1:c.1842G>T | ENSP00000507003.1:n.1842G>T | |
| ENST00000268097.10:c.1511G>T MANE Select | ENSP00000268097.6:p.Arg504Leu | |
| ENST00000268097.9:c.1511G>T | ENSP00000268097.5:p.Arg504Leu | |
| ENST00000379915.4:c.593G>T | ENSP00000478716.1:p.Arg198Leu | |
| ENST00000564677.5:n.303G>T | ||
| ENST00000565873.1:n.422G>T | ||
| ENST00000566304.5:c.1544G>T | ENSP00000455114.1:p.Arg515Leu | |
| ENST00000567027.5:c.1126G>T | ||
| ENST00000567159.5:c.1511G>T | ENSP00000456489.1:p.Arg504Leu | |
| ENST00000567411.5:c.*1032G>T | ENSP00000455545.1:n.*1032G>T | |
| ENST00000568777.5:n.6731G>T | ||
| ENST00000569116.1:n.218G>T | ||
| NM_000520.4:c.1511G>T | NP_000511.2:p.Arg504Leu | |
| NM_000520.5:c.1511G>T | NP_000511.2:p.Arg504Leu | |
| NM_001318825.1:c.1544G>T | NP_001305754.1:p.Arg515Leu | |
| NR_134869.1:n.1755G>T | ||
| NM_000520.6:c.1511G>T MANE Select | NP_000511.2:p.Arg504Leu | |
| NM_001318825.2:c.1544G>T | NP_001305754.1:p.Arg515Leu | |
| NR_134869.2:n.1296G>T | ||
| NR_134869.3:n.1296G>T |