Canonical Allele Identifier: CA1401205722
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528966_129528967delinsAC , CM000665.2:g.129528966_129528967delinsAC GRCh38
NC_000003.11:g.129247809_129247810delinsAC , CM000665.1:g.129247809_129247810delinsAC GRCh37
NC_000003.10:g.130730499_130730500delinsAC NCBI36
NG_009115.1:g.5328_5329delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.233_234delinsAC MANE Select ENSP00000296271.3:p.Asn78=
ENST00000296271.3:c.233_234delinsAC ENSP00000296271.3:p.Asn78=
NM_000539.3:c.233_234delinsAC MANE Select NP_000530.1:p.Asn78=