Canonical Allele Identifier: CA354495432

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129247632T>G (hg19) ; chr3:g.129528789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129528789T>G , CM000665.2:g.129528789T>G	GRCh38
NC_000003.11:g.129247632T>G , CM000665.1:g.129247632T>G	GRCh37
NC_000003.10:g.130730322T>G	NCBI36
NG_009115.1:g.5151T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.56T>G MANE Select	ENSP00000296271.3:p.Val19Gly
ENST00000296271.3:c.56T>G	ENSP00000296271.3:p.Val19Gly
NM_000539.3:c.56T>G MANE Select	NP_000530.1:p.Val19Gly