Canonical Allele Identifier: CA354470776

Gene: RHO

Linked Data

• gnomAD v4: 3-129532719-G-A
• MyVariant Identifiers: chr3:g.129251562G>A (hg19) ; chr3:g.129532719G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532719G>A , CM000665.2:g.129532719G>A	GRCh38
NC_000003.11:g.129251562G>A , CM000665.1:g.129251562G>A	GRCh37
NC_000003.10:g.130734252G>A	NCBI36
NG_009115.1:g.9081G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.883G>A MANE Select	ENSP00000296271.3:p.Ala295Thr
ENST00000296271.3:c.883G>A	ENSP00000296271.3:p.Ala295Thr
NM_000539.3:c.883G>A MANE Select	NP_000530.1:p.Ala295Thr