Linked Data
ClinVar Variation Id:
97247
dbSNP Id:
rs72556293
COSMIC:
COSM4943622
PubMed:
PMID:8260194
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38403625A>G , CM000685.2:g.38403625A>G | GRCh38 |
| NC_000023.10:g.38262878A>G , CM000685.1:g.38262878A>G | GRCh37 |
| NC_000023.9:g.38147822A>G | NCBI36 |
| NG_008471.1:g.56143A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.548A>G MANE Select | ENSP00000039007.4:p.Tyr183Cys | |
| ENST00000643344.1:c.*298A>G | ENSP00000496606.1:n.*298A>G | |
| ENST00000039007.4:c.548A>G | ENSP00000039007.4:p.Tyr183Cys | |
| ENST00000465127.1:c.172-262496A>G | ENSP00000417050.1:n.172-262496A>G | |
| ENST00000488812.1:n.585A>G | ||
| NM_000531.5:c.548A>G | NP_000522.3:p.Tyr183Cys | |
| XM_017029556.1:c.548A>G | XP_016885045.1:p.Tyr183Cys | |
| NM_000531.6:c.548A>G MANE Select | NP_000522.3:p.Tyr183Cys |