Canonical Allele Identifier: CA354497024

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129247932T>G (hg19) ; chr3:g.129529089T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529089T>G , CM000665.2:g.129529089T>G	GRCh38
NC_000003.11:g.129247932T>G , CM000665.1:g.129247932T>G	GRCh37
NC_000003.10:g.130730622T>G	NCBI36
NG_009115.1:g.5451T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.356T>G MANE Select	ENSP00000296271.3:p.Leu119Arg
ENST00000296271.3:c.356T>G	ENSP00000296271.3:p.Leu119Arg
NM_000539.3:c.356T>G MANE Select	NP_000530.1:p.Leu119Arg