Canonical Allele Identifier: CA354470735
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532714T>A , CM000665.2:g.129532714T>A GRCh38
NC_000003.11:g.129251557T>A , CM000665.1:g.129251557T>A GRCh37
NC_000003.10:g.130734247T>A NCBI36
NG_009115.1:g.9076T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.878T>A MANE Select ENSP00000296271.3:p.Phe293Tyr
ENST00000296271.3:c.878T>A ENSP00000296271.3:p.Phe293Tyr
NM_000539.3:c.878T>A MANE Select NP_000530.1:p.Phe293Tyr