Canonical Allele Identifier: CA354470834

Gene: RHO

Linked Data

• dbSNP Id: rs1578281089
• MyVariant Identifiers: chr3:g.129251572C>A (hg19) ; chr3:g.129532729C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532729C>A , CM000665.2:g.129532729C>A	GRCh38
NC_000003.11:g.129251572C>A , CM000665.1:g.129251572C>A	GRCh37
NC_000003.10:g.130734262C>A	NCBI36
NG_009115.1:g.9091C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.893C>A MANE Select	ENSP00000296271.3:p.Ala298Asp
ENST00000296271.3:c.893C>A	ENSP00000296271.3:p.Ala298Asp
NM_000539.3:c.893C>A MANE Select	NP_000530.1:p.Ala298Asp