Canonical Allele Identifier: CA354498330

Gene: RHO

Linked Data

• gnomAD v4: 3-129530969-A-G
• MyVariant Identifiers: chr3:g.129249812A>G (hg19) ; chr3:g.129530969A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530969A>G , CM000665.2:g.129530969A>G	GRCh38
NC_000003.11:g.129249812A>G , CM000665.1:g.129249812A>G	GRCh37
NC_000003.10:g.130732502A>G	NCBI36
NG_009115.1:g.7331A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.455A>G MANE Select	ENSP00000296271.3:p.His152Arg
ENST00000296271.3:c.455A>G	ENSP00000296271.3:p.His152Arg
NM_000539.3:c.455A>G MANE Select	NP_000530.1:p.His152Arg