Canonical Allele Identifier: CA1401209096

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530806_129530807delinsCT , CM000665.2:g.129530806_129530807delinsCT	GRCh38
NC_000003.11:g.129249649_129249650delinsCT , CM000665.1:g.129249649_129249650delinsCT	GRCh37
NC_000003.10:g.130732339_130732340delinsCT	NCBI36
NG_009115.1:g.7168_7169delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.362-70_362-69delinsCT MANE Select	ENSP00000296271.3:n.362-70_362-69delinsCT
ENST00000296271.3:c.362-70_362-69delinsCT	ENSP00000296271.3:n.362-70_362-69delinsCT
NM_000539.3:c.362-70_362-69delinsCT MANE Select	NP_000530.1:n.362-70_362-69delinsCT