Canonical Allele Identifier: CA354470352

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129251461T>A (hg19) ; chr3:g.129532618T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532618T>A , CM000665.2:g.129532618T>A	GRCh38
NC_000003.11:g.129251461T>A , CM000665.1:g.129251461T>A	GRCh37
NC_000003.10:g.130734151T>A	NCBI36
NG_009115.1:g.8980T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.782T>A MANE Select	ENSP00000296271.3:p.Phe261Tyr
ENST00000296271.3:c.782T>A	ENSP00000296271.3:p.Phe261Tyr
NM_000539.3:c.782T>A MANE Select	NP_000530.1:p.Phe261Tyr