Canonical Allele Identifier: CA354497828

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129249719G>A (hg19) ; chr3:g.129530876G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530876G>A , CM000665.2:g.129530876G>A	GRCh38
NC_000003.11:g.129249719G>A , CM000665.1:g.129249719G>A	GRCh37
NC_000003.10:g.130732409G>A	NCBI36
NG_009115.1:g.7238G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.362G>A MANE Select	ENSP00000296271.3:p.Gly121Asp
ENST00000296271.3:c.362G>A	ENSP00000296271.3:p.Gly121Asp
NM_000539.3:c.362G>A MANE Select	NP_000530.1:p.Gly121Asp