Linked Data
ClinVar Variation Id:
1574
ClinVar RCV Id:
RCV000001640
dbSNP Id:
rs137852866
PubMed:
PMID:10942115
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121846919A>C , CM000674.2:g.121846919A>C | GRCh38 |
| NC_000012.11:g.122284825A>C , CM000674.1:g.122284825A>C | GRCh37 |
| NC_000012.10:g.120769208A>C | NCBI36 |
| NG_016461.1:g.46693T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000289004.8:c.774T>G MANE Select | ENSP00000289004.4:p.Tyr258Ter | |
| ENST00000543163.5:c.657T>G | ENSP00000441677.1:p.Tyr219Ter | |
| NM_001171993.1:c.657T>G | NP_001165464.1:p.Tyr219Ter | |
| NM_002150.2:c.774T>G | NP_002141.1:p.Tyr258Ter | |
| NM_002150.3:c.774T>G MANE Select | NP_002141.2:p.Tyr258Ter | |
| NM_001171993.2:c.657T>G | NP_001165464.1:p.Tyr219Ter |