Canonical Allele Identifier: CA1401208850
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530546_129530547delinsAC , CM000665.2:g.129530546_129530547delinsAC GRCh38
NC_000003.11:g.129249389_129249390delinsAC , CM000665.1:g.129249389_129249390delinsAC GRCh37
NC_000003.10:g.130732079_130732080delinsAC NCBI36
NG_009115.1:g.6908_6909delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-330_362-329delinsAC MANE Select ENSP00000296271.3:n.362-330_362-329delinsAC
ENST00000296271.3:c.362-330_362-329delinsAC ENSP00000296271.3:n.362-330_362-329delinsAC
NM_000539.3:c.362-330_362-329delinsAC MANE Select NP_000530.1:n.362-330_362-329delinsAC