Linked Data
dbSNP Id:
rs778448610
ExAC:
3:120360522 C / T
gnomAD v2:
3-120360522-C-T
gnomAD v4:
3-120641675-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.120641675C>T , CM000665.2:g.120641675C>T | GRCh38 |
| NC_000003.11:g.120360522C>T , CM000665.1:g.120360522C>T | GRCh37 |
| NC_000003.10:g.121843212C>T | NCBI36 |
| NG_011957.1:g.45807G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283871.10:c.793G>A MANE Select | ENSP00000283871.5:p.Val265Ile | |
| ENST00000283871.9:c.793G>A | ENSP00000283871.5:p.Val265Ile | |
| ENST00000470321.1:n.133G>A | ||
| ENST00000475447.2:c.221G>A | ||
| ENST00000492108.5:c.199G>A | ENSP00000419838.1:p.Val67Ile | |
| ENST00000494453.1:c.213G>A | ||
| NM_000187.3:c.793G>A | NP_000178.2:p.Val265Ile | |
| XM_005247412.1:c.568G>A | XP_005247469.1:p.Val190Ile | |
| XM_005247413.1:c.793G>A | XP_005247470.1:p.Val265Ile | |
| XM_011512746.1:c.793G>A | XP_011511048.1:p.Val265Ile | |
| XM_005247412.2:c.568G>A | XP_005247469.1:p.Val190Ile | |
| XM_005247413.2:c.793G>A | XP_005247470.1:p.Val265Ile | |
| XM_011512746.2:c.793G>A | XP_011511048.1:p.Val265Ile | |
| XM_017006277.2:c.370G>A | XP_016861766.1:p.Val124Ile | |
| NM_000187.4:c.793G>A MANE Select | NP_000178.2:p.Val265Ile |