Canonical Allele Identifier: CA2758363943
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531079_129531080insAGA , CM000665.2:g.129531079_129531080insAGA GRCh38
NC_000003.11:g.129249922_129249923insAGA , CM000665.1:g.129249922_129249923insAGA GRCh37
NC_000003.10:g.130732612_130732613insAGA NCBI36
NG_009115.1:g.7441_7442insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.530+35_530+36insAGA MANE Select ENSP00000296271.3:n.530+35_530+36insAGA
ENST00000296271.3:c.530+35_530+36insAGA ENSP00000296271.3:n.530+35_530+36insAGA
NM_000539.3:c.530+35_530+36insAGA MANE Select NP_000530.1:n.530+35_530+36insAGA