Linked Data
ClinVar Variation Id:
15266
ClinVar RCV Id:
RCV000016490
dbSNP Id:
rs33928092
PubMed:
PMID:6547119
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225686A>T , CM000673.2:g.5225686A>T | GRCh38 |
| NC_000011.9:g.5246916A>T , CM000673.1:g.5246916A>T | GRCh37 |
| NC_000011.8:g.5203492A>T | NCBI36 |
| NG_000007.3:g.71930T>A | |
| NG_059281.1:g.6386T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.356T>A | ENSP00000494175.1:p.Phe119Tyr | |
| ENST00000335295.4:c.356T>A MANE Select | ENSP00000333994.3:p.Phe119Tyr | |
| ENST00000475226.1:n.288T>A | ||
| ENST00000633227.1:c.*172T>A | ENSP00000488004.1:n.*172T>A | |
| NM_000518.4:c.356T>A | NP_000509.1:p.Phe119Tyr | |
| NM_000518.5:c.356T>A MANE Select | NP_000509.1:p.Phe119Tyr |