Canonical Allele Identifier: CA2758363942

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129531078_129531079insA , CM000665.2:g.129531078_129531079insA	GRCh38
NC_000003.11:g.129249921_129249922insA , CM000665.1:g.129249921_129249922insA	GRCh37
NC_000003.10:g.130732611_130732612insA	NCBI36
NG_009115.1:g.7440_7441insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.530+34_530+35insA MANE Select	ENSP00000296271.3:n.530+34_530+35insA
ENST00000296271.3:c.530+34_530+35insA	ENSP00000296271.3:n.530+34_530+35insA
NM_000539.3:c.530+34_530+35insA MANE Select	NP_000530.1:n.530+34_530+35insA