Canonical Allele Identifier: CA2758363682
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529168_129529169insACA , CM000665.2:g.129529168_129529169insACA GRCh38
NC_000003.11:g.129248011_129248012insACA , CM000665.1:g.129248011_129248012insACA GRCh37
NC_000003.10:g.130730701_130730702insACA NCBI36
NG_009115.1:g.5530_5531insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+74_361+75insACA MANE Select ENSP00000296271.3:n.361+74_361+75insACA
ENST00000296271.3:c.361+74_361+75insACA ENSP00000296271.3:n.361+74_361+75insACA
NM_000539.3:c.361+74_361+75insACA MANE Select NP_000530.1:n.361+74_361+75insACA