Linked Data
ClinVar Variation Id:
16391
dbSNP Id:
rs121909623
gnomAD v2:
4-155488840-C-T
gnomAD v4:
4-154567688-C-T
COSMIC:
COSM1207016
PubMed:
PMID:11468164
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.154567688C>T , CM000666.2:g.154567688C>T | GRCh38 |
| NC_000004.11:g.155488840C>T , CM000666.1:g.155488840C>T | GRCh37 |
| NC_000004.10:g.155708290C>T | NCBI36 |
| NG_008833.1:g.9709C>T , LRG_558:g.9709C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302068.9:c.586C>T MANE Select | ENSP00000306099.4:p.Arg196Cys | |
| ENST00000302068.8:c.586C>T | ENSP00000306099.4:p.Arg196Cys | |
| ENST00000473984.1:n.499C>T | ||
| ENST00000502545.5:n.567C>T | ||
| ENST00000509493.1:c.-72C>T | ENSP00000426757.1:n.-72C>T | |
| NM_001184741.1:c.409C>T | NP_001171670.1:p.Arg137Cys | |
| NM_005141.4:c.586C>T , LRG_558t1:c.586C>T | NP_005132.2:p.Arg196Cys | |
| NM_001382759.1:c.454C>T | NP_001369688.1:p.Arg152Cys | |
| NM_001382760.1:c.586C>T | NP_001369689.1:p.Arg196Cys | |
| NM_001382761.1:c.586C>T | NP_001369690.1:p.Arg196Cys | |
| NM_001382762.1:c.586C>T | NP_001369691.1:p.Arg196Cys | |
| NM_001382763.1:c.586C>T | NP_001369692.1:p.Arg196Cys | |
| NM_001382764.1:c.586C>T | NP_001369693.1:p.Arg196Cys | |
| NM_001382765.1:c.586C>T | NP_001369694.1:p.Arg196Cys | |
| NM_005141.5:c.586C>T MANE Select | NP_005132.2:p.Arg196Cys |