Linked Data
ClinVar Variation Id:
371169
ClinVar RCV Id:
RCV000409611
dbSNP Id:
rs762374961
gnomAD v4:
15-72346235-C-T
PubMed:
PMID:23852624
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72346235C>T , CM000677.2:g.72346235C>T | GRCh38 |
| NC_000015.9:g.72638576C>T , CM000677.1:g.72638576C>T | GRCh37 |
| NC_000015.8:g.70425630C>T | NCBI36 |
| NG_009017.1:g.34945G>A | |
| NG_009017.2:g.34945G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567027.6:c.*81G>A | ENSP00000457521.2:n.*81G>A | |
| ENST00000682061.1:c.*1083G>A | ENSP00000508316.1:n.*1083G>A | |
| ENST00000682064.1:n.964G>A | ||
| ENST00000682177.1:c.1464G>A | ENSP00000507409.1:n.1464G>A | |
| ENST00000682235.1:n.760G>A | ||
| ENST00000682461.1:c.1527G>A | ENSP00000507308.1:n.1527G>A | |
| ENST00000682653.1:n.1741G>A | ||
| ENST00000682657.1:c.*574G>A | ENSP00000507753.1:n.*574G>A | |
| ENST00000682721.1:c.*1224G>A | ENSP00000507535.1:n.*1224G>A | |
| ENST00000682843.1:c.*1062G>A | ENSP00000508173.1:n.*1062G>A | |
| ENST00000683003.1:c.*574G>A | ENSP00000507576.1:n.*574G>A | |
| ENST00000683133.1:c.1605G>A | ENSP00000508108.1:n.1605G>A | |
| ENST00000683243.1:c.*574G>A | ENSP00000507042.1:n.*574G>A | |
| ENST00000683463.1:c.*226G>A | ENSP00000507986.1:n.*226G>A | |
| ENST00000683548.1:n.1195G>A | ||
| ENST00000683579.1:c.*1319G>A | ENSP00000506867.1:n.*1319G>A | |
| ENST00000683587.1:n.1268G>A | ||
| ENST00000683681.1:c.1421G>A | ENSP00000508110.1:p.Ter474= | |
| ENST00000683735.1:c.*1135G>A | ENSP00000508336.1:n.*1135G>A | |
| ENST00000683853.1:c.*226G>A | ENSP00000506834.1:n.*226G>A | |
| ENST00000683860.1:c.1421G>A | ENSP00000507179.1:p.Trp474Ter | |
| ENST00000683884.1:c.*64G>A | ENSP00000507004.1:n.*64G>A | |
| ENST00000684041.1:c.1421G>A | ENSP00000508382.1:p.Trp474Ter | |
| ENST00000684125.1:c.*81G>A | ENSP00000507320.1:n.*81G>A | |
| ENST00000684203.1:n.3186G>A | ||
| ENST00000684231.1:c.*831G>A | ENSP00000507748.1:n.*831G>A | |
| ENST00000684263.1:c.*361G>A | ENSP00000508369.1:n.*361G>A | |
| ENST00000684305.1:c.1869G>A | ENSP00000506819.1:n.1869G>A | |
| ENST00000684415.1:c.*288G>A | ENSP00000507227.1:n.*288G>A | |
| ENST00000684520.1:c.1421G>A | ENSP00000506826.1:p.Trp474Ter | |
| ENST00000684602.1:c.*1087G>A | ENSP00000507996.1:n.*1087G>A | |
| ENST00000684667.1:c.1752G>A | ENSP00000507003.1:n.1752G>A | |
| ENST00000268097.10:c.1421G>A MANE Select | ENSP00000268097.6:p.Trp474Ter | |
| ENST00000268097.9:c.1421G>A | ENSP00000268097.5:p.Trp474Ter | |
| ENST00000379915.4:c.503G>A | ENSP00000478716.1:p.Trp168Ter | |
| ENST00000563762.5:c.916G>A | ENSP00000456346.1:n.916G>A | |
| ENST00000566304.5:c.1454G>A | ENSP00000455114.1:p.Trp485Ter | |
| ENST00000566672.5:c.*831G>A | ENSP00000457037.1:n.*831G>A | |
| ENST00000567027.5:c.1036G>A | ||
| ENST00000567159.5:c.1421G>A | ENSP00000456489.1:p.Trp474Ter | |
| ENST00000567411.5:c.*942G>A | ENSP00000455545.1:n.*942G>A | |
| ENST00000568777.5:n.6641G>A | ||
| ENST00000569410.5:c.*226G>A | ENSP00000457125.1:n.*226G>A | |
| NM_000520.4:c.1421G>A | NP_000511.2:p.Trp474Ter | |
| NM_000520.5:c.1421G>A | NP_000511.2:p.Trp474Ter | |
| NM_001318825.1:c.1454G>A | NP_001305754.1:p.Trp485Ter | |
| NR_134869.1:n.1665G>A | ||
| NM_000520.6:c.1421G>A MANE Select | NP_000511.2:p.Trp474Ter | |
| NM_001318825.2:c.1454G>A | NP_001305754.1:p.Trp485Ter | |
| NR_134869.2:n.1206G>A | ||
| NR_134869.3:n.1206G>A |