ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25241585C>T , CM000664.2:g.25241585C>T | GRCh38 |
| NC_000002.11:g.25464454C>T , CM000664.1:g.25464454C>T | GRCh37 |
| NC_000002.10:g.25317958C>T | NCBI36 |
| NG_029465.2:g.106006G>A , LRG_459:g.106006G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474887.6:c.378G>A | ||
| ENST00000683393.1:c.1205G>A | ENSP00000508654.1:n.1205G>A | |
| ENST00000683760.1:c.1390G>A | ENSP00000507765.1:p.Val464Ile | |
| ENST00000321117.10:c.2059G>A MANE Select | ENSP00000324375.5:p.Val687Ile | |
| ENST00000264709.7:c.2059G>A | ENSP00000264709.3:p.Val687Ile | |
| ENST00000321117.9:c.2059G>A | ENSP00000324375.5:p.Val687Ile | |
| ENST00000380746.8:c.1492G>A | ENSP00000370122.4:p.Val498Ile | |
| ENST00000380756.7:c.2059G>A | ENSP00000370132.3:p.Val687Ile | |
| ENST00000402667.1:c.1390G>A | ENSP00000384237.1:p.Val464Ile | |
| ENST00000461228.1:n.278G>A | ||
| ENST00000466601.5:n.431G>A | ||
| ENST00000474887.5:n.378G>A | ||
| ENST00000482935.5:n.83-855G>A | ||
| ENST00000491288.5:n.196G>A | ||
| NM_022552.4:c.2059G>A , LRG_459t1:c.2059G>A | NP_072046.2:p.Val687Ile | |
| NM_153759.3:c.1492G>A , LRG_459t2:c.1492G>A | NP_715640.2:p.Val498Ile | |
| NM_175629.2:c.2059G>A , LRG_459t4:c.2059G>A | NP_783328.1:p.Val687Ile | |
| XM_005264175.3:c.2059G>A | XP_005264232.1:p.Val687Ile | |
| XM_005264177.3:c.1390G>A | XP_005264234.1:p.Val464Ile | |
| XM_006711957.2:c.2059G>A | XP_006712020.1:p.Val687Ile | |
| XM_006711958.2:c.1615G>A | XP_006712021.1:p.Val539Ile | |
| XM_011532662.1:c.1912G>A | XP_011530964.1:p.Val638Ile | |
| XM_011532663.1:c.1894G>A | XP_011530965.1:p.Val632Ile | |
| XM_011532664.1:c.2059G>A | XP_011530966.1:p.Val687Ile | |
| XM_011532665.1:c.1603G>A | XP_011530967.1:p.Val535Ile | |
| XM_011532666.1:c.1531G>A | XP_011530968.1:p.Val511Ile | |
| XM_011532667.1:c.1390G>A | XP_011530969.1:p.Val464Ile | |
| XM_011532668.1:c.2059G>A | XP_011530970.1:p.Val687Ile | |
| NM_001320893.1:c.1603G>A | NP_001307822.1:p.Val535Ile | |
| NR_135490.1:n.2397G>A | ||
| XM_005264175.5:c.2059G>A | XP_005264232.1:p.Val687Ile | |
| XM_005264177.4:c.1390G>A | XP_005264234.1:p.Val464Ile | |
| XM_011532662.2:c.1912G>A | XP_011530964.1:p.Val638Ile | |
| XM_011532663.2:c.1894G>A | XP_011530965.1:p.Val632Ile | |
| XM_011532664.2:c.2059G>A | XP_011530966.1:p.Val687Ile | |
| XM_011532666.2:c.1531G>A | XP_011530968.1:p.Val511Ile | |
| XM_011532667.3:c.1390G>A | XP_011530969.1:p.Val464Ile | |
| XM_017003526.1:c.2059G>A | XP_016859015.1:p.Val687Ile | |
| XM_017003527.1:c.1390G>A | XP_016859016.1:p.Val464Ile | |
| XR_001738657.1:n.2336G>A | ||
| NM_001375819.1:c.1390G>A | NP_001362748.1:p.Val464Ile | |
| NR_135490.2:n.2290G>A | ||
| NM_022552.5:c.2059G>A MANE Select | NP_072046.2:p.Val687Ile |