Canonical Allele Identifier: CA1401208260
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530531_129530532delinsAC , CM000665.2:g.129530531_129530532delinsAC GRCh38
NC_000003.11:g.129249374_129249375delinsAC , CM000665.1:g.129249374_129249375delinsAC GRCh37
NC_000003.10:g.130732064_130732065delinsAC NCBI36
NG_009115.1:g.6893_6894delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-345_362-344delinsAC MANE Select ENSP00000296271.3:n.362-345_362-344delinsAC
ENST00000296271.3:c.362-345_362-344delinsAC ENSP00000296271.3:n.362-345_362-344delinsAC
NM_000539.3:c.362-345_362-344delinsAC MANE Select NP_000530.1:n.362-345_362-344delinsAC