Canonical Allele Identifier: CA82648911

Gene: RHO

Linked Data

• dbSNP Id: rs964869603
• MyVariant Identifiers: chr3:g.129249931G>A (hg19) ; chr3:g.129531088G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129531088G>A , CM000665.2:g.129531088G>A	GRCh38
NC_000003.11:g.129249931G>A , CM000665.1:g.129249931G>A	GRCh37
NC_000003.10:g.130732621G>A	NCBI36
NG_009115.1:g.7450G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.530+44G>A MANE Select	ENSP00000296271.3:n.530+44G>A
ENST00000296271.3:c.530+44G>A	ENSP00000296271.3:n.530+44G>A
NM_000539.3:c.530+44G>A MANE Select	NP_000530.1:n.530+44G>A