Linked Data
ClinVar Variation Id:
2168862
dbSNP Id:
rs375019490
gnomAD v2:
15-72638615-C-A
gnomAD v4:
15-72346274-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72346274C>A , CM000677.2:g.72346274C>A | GRCh38 |
| NC_000015.9:g.72638615C>A , CM000677.1:g.72638615C>A | GRCh37 |
| NC_000015.8:g.70425669C>A | NCBI36 |
| NG_009017.1:g.34906G>T | |
| NG_009017.2:g.34906G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.*42G>T | ENSP00000457521.2:n.*42G>T | |
| ENST00000682061.1:c.*1044G>T | ENSP00000508316.1:n.*1044G>T | |
| ENST00000682064.1:n.925G>T | ||
| ENST00000682177.1:c.1425G>T | ENSP00000507409.1:n.1425G>T | |
| ENST00000682235.1:n.721G>T | ||
| ENST00000682461.1:c.1488G>T | ENSP00000507308.1:n.1488G>T | |
| ENST00000682653.1:n.1702G>T | ||
| ENST00000682657.1:c.*535G>T | ENSP00000507753.1:n.*535G>T | |
| ENST00000682721.1:c.*1185G>T | ENSP00000507535.1:n.*1185G>T | |
| ENST00000682843.1:c.*1023G>T | ENSP00000508173.1:n.*1023G>T | |
| ENST00000683003.1:c.*535G>T | ENSP00000507576.1:n.*535G>T | |
| ENST00000683133.1:c.1566G>T | ENSP00000508108.1:n.1566G>T | |
| ENST00000683243.1:c.*535G>T | ENSP00000507042.1:n.*535G>T | |
| ENST00000683463.1:c.*187G>T | ENSP00000507986.1:n.*187G>T | |
| ENST00000683548.1:n.1156G>T | ||
| ENST00000683579.1:c.*1280G>T | ENSP00000506867.1:n.*1280G>T | |
| ENST00000683587.1:n.1229G>T | ||
| ENST00000683681.1:c.1382G>T | ENSP00000508110.1:p.Gly461Val | |
| ENST00000683735.1:c.*1096G>T | ENSP00000508336.1:n.*1096G>T | |
| ENST00000683853.1:c.*187G>T | ENSP00000506834.1:n.*187G>T | |
| ENST00000683860.1:c.1382G>T | ENSP00000507179.1:p.Gly461Val | |
| ENST00000683884.1:c.*25G>T | ENSP00000507004.1:n.*25G>T | |
| ENST00000684041.1:c.1382G>T | ENSP00000508382.1:p.Gly461Val | |
| ENST00000684125.1:c.*42G>T | ENSP00000507320.1:n.*42G>T | |
| ENST00000684203.1:n.3147G>T | ||
| ENST00000684231.1:c.*792G>T | ENSP00000507748.1:n.*792G>T | |
| ENST00000684263.1:c.*322G>T | ENSP00000508369.1:n.*322G>T | |
| ENST00000684305.1:c.1830G>T | ENSP00000506819.1:n.1830G>T | |
| ENST00000684415.1:c.*249G>T | ENSP00000507227.1:n.*249G>T | |
| ENST00000684520.1:c.1382G>T | ENSP00000506826.1:p.Gly461Val | |
| ENST00000684602.1:c.*1048G>T | ENSP00000507996.1:n.*1048G>T | |
| ENST00000684667.1:c.1713G>T | ENSP00000507003.1:n.1713G>T | |
| ENST00000268097.10:c.1382G>T MANE Select | ENSP00000268097.6:p.Gly461Val | |
| ENST00000268097.9:c.1382G>T | ENSP00000268097.5:p.Gly461Val | |
| ENST00000379915.4:c.464G>T | ENSP00000478716.1:p.Gly155Val | |
| ENST00000563762.5:c.877G>T | ENSP00000456346.1:n.877G>T | |
| ENST00000566304.5:c.1415G>T | ENSP00000455114.1:p.Gly472Val | |
| ENST00000566672.5:c.*792G>T | ENSP00000457037.1:n.*792G>T | |
| ENST00000567027.5:c.997G>T | ||
| ENST00000567159.5:c.1382G>T | ENSP00000456489.1:p.Gly461Val | |
| ENST00000567411.5:c.*903G>T | ENSP00000455545.1:n.*903G>T | |
| ENST00000568777.5:n.6602G>T | ||
| ENST00000569410.5:c.*187G>T | ENSP00000457125.1:n.*187G>T | |
| NM_000520.4:c.1382G>T | NP_000511.2:p.Gly461Val | |
| NM_000520.5:c.1382G>T | NP_000511.2:p.Gly461Val | |
| NM_001318825.1:c.1415G>T | NP_001305754.1:p.Gly472Val | |
| NR_134869.1:n.1626G>T | ||
| NM_000520.6:c.1382G>T MANE Select | NP_000511.2:p.Gly461Val | |
| NM_001318825.2:c.1415G>T | NP_001305754.1:p.Gly472Val | |
| NR_134869.2:n.1167G>T | ||
| NR_134869.3:n.1167G>T |