Linked Data
ClinVar Variation Id:
652052
ClinVar RCV Id:
RCV000807538
dbSNP Id:
rs551170184
ExAC:
6:35423931 G / T
gnomAD v2:
6-35423931-G-T
gnomAD v3:
6-35456154-G-T
gnomAD v4:
6-35456154-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35456154G>T , CM000668.2:g.35456154G>T | GRCh38 |
| NC_000006.11:g.35423931G>T , CM000668.1:g.35423931G>T | GRCh37 |
| NC_000006.10:g.35531909G>T | NCBI36 |
| NG_011708.1:g.8794G>T , LRG_498:g.8794G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696264.1:c.656G>T | ENSP00000512511.1:p.Arg219Ile | |
| ENST00000696265.1:c.656G>T | ENSP00000512512.1:p.Arg219Ile | |
| ENST00000696266.1:c.374G>T | ENSP00000512513.1:p.Arg125Ile | |
| ENST00000696267.1:n.296G>T | ||
| ENST00000229769.3:c.656G>T MANE Select | ENSP00000229769.2:p.Arg219Ile | |
| ENST00000648059.1:c.656G>T | ENSP00000497902.1:p.Arg219Ile | |
| ENST00000229769.2:c.656G>T | ENSP00000229769.2:p.Arg219Ile | |
| NM_021922.2:c.656G>T , LRG_498t1:c.656G>T | NP_068741.1:p.Arg219Ile | |
| XM_005248885.2:c.656G>T | XP_005248942.1:p.Arg219Ile | |
| XM_005248886.2:c.656G>T | XP_005248943.1:p.Arg219Ile | |
| XM_005248887.2:c.656G>T | XP_005248944.1:p.Arg219Ile | |
| XM_005248888.2:c.656G>T | XP_005248945.1:p.Arg219Ile | |
| XM_011514343.1:c.362G>T | XP_011512645.1:p.Arg121Ile | |
| XM_011514344.1:c.362G>T | XP_011512646.1:p.Arg121Ile | |
| XM_005248888.3:c.656G>T | XP_005248945.1:p.Arg219Ile | |
| XM_011514343.2:c.362G>T | XP_011512645.1:p.Arg121Ile | |
| XR_001743226.1:n.863G>T | ||
| XR_002956267.1:n.863G>T | ||
| NM_021922.3:c.656G>T MANE Select | NP_068741.1:p.Arg219Ile |