Linked Data
ClinVar Variation Id:
8710
ClinVar RCV Id:
RCV000009248
dbSNP Id:
rs121434506
ExAC:
6:35423696 C / T
gnomAD v2:
6-35423696-C-T
gnomAD v3:
6-35455919-C-T
gnomAD v4:
6-35455919-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35455919C>T , CM000668.2:g.35455919C>T | GRCh38 |
| NC_000006.11:g.35423696C>T , CM000668.1:g.35423696C>T | GRCh37 |
| NC_000006.10:g.35531674C>T | NCBI36 |
| NG_011708.1:g.8559C>T , LRG_498:g.8559C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696264.1:c.421C>T | ENSP00000512511.1:p.Arg141Ter | |
| ENST00000696265.1:c.421C>T | ENSP00000512512.1:p.Arg141Ter | |
| ENST00000696266.1:c.139C>T | ENSP00000512513.1:p.Arg47Ter | |
| ENST00000696267.1:n.61C>T | ||
| ENST00000229769.3:c.421C>T MANE Select | ENSP00000229769.2:p.Arg141Ter | |
| ENST00000648059.1:c.421C>T | ENSP00000497902.1:p.Arg141Ter | |
| ENST00000229769.2:c.421C>T | ENSP00000229769.2:p.Arg141Ter | |
| NM_021922.2:c.421C>T , LRG_498t1:c.421C>T | NP_068741.1:p.Arg141Ter | |
| XM_005248885.2:c.421C>T | XP_005248942.1:p.Arg141Ter | |
| XM_005248886.2:c.421C>T | XP_005248943.1:p.Arg141Ter | |
| XM_005248887.2:c.421C>T | XP_005248944.1:p.Arg141Ter | |
| XM_005248888.2:c.421C>T | XP_005248945.1:p.Arg141Ter | |
| XM_011514343.1:c.127C>T | XP_011512645.1:p.Arg43Ter | |
| XM_011514344.1:c.127C>T | XP_011512646.1:p.Arg43Ter | |
| XM_005248888.3:c.421C>T | XP_005248945.1:p.Arg141Ter | |
| XM_011514343.2:c.127C>T | XP_011512645.1:p.Arg43Ter | |
| XR_001743226.1:n.628C>T | ||
| XR_002956267.1:n.628C>T | ||
| NM_021922.3:c.421C>T MANE Select | NP_068741.1:p.Arg141Ter |