Canonical Allele Identifier: CA1401208834
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530542_129530543delinsAC , CM000665.2:g.129530542_129530543delinsAC GRCh38
NC_000003.11:g.129249385_129249386delinsAC , CM000665.1:g.129249385_129249386delinsAC GRCh37
NC_000003.10:g.130732075_130732076delinsAC NCBI36
NG_009115.1:g.6904_6905delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-334_362-333delinsAC MANE Select ENSP00000296271.3:n.362-334_362-333delinsAC
ENST00000296271.3:c.362-334_362-333delinsAC ENSP00000296271.3:n.362-334_362-333delinsAC
NM_000539.3:c.362-334_362-333delinsAC MANE Select NP_000530.1:n.362-334_362-333delinsAC