Canonical Allele Identifier: CA2758363822

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529265_129529266insAGA , CM000665.2:g.129529265_129529266insAGA	GRCh38
NC_000003.11:g.129248108_129248109insAGA , CM000665.1:g.129248108_129248109insAGA	GRCh37
NC_000003.10:g.130730798_130730799insAGA	NCBI36
NG_009115.1:g.5627_5628insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+171_361+172insAGA MANE Select	ENSP00000296271.3:n.361+171_361+172insAGA
ENST00000296271.3:c.361+171_361+172insAGA	ENSP00000296271.3:n.361+171_361+172insAGA
NM_000539.3:c.361+171_361+172insAGA MANE Select	NP_000530.1:n.361+171_361+172insAGA