Canonical Allele Identifier: CA2758361758
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532879_129532880insAC , CM000665.2:g.129532879_129532880insAC GRCh38
NC_000003.11:g.129251722_129251723insAC , CM000665.1:g.129251722_129251723insAC GRCh37
NC_000003.10:g.130734412_130734413insAC NCBI36
NG_009115.1:g.9241_9242insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.936+107_936+108insAC MANE Select ENSP00000296271.3:n.936+107_936+108insAC
ENST00000296271.3:c.936+107_936+108insAC ENSP00000296271.3:n.936+107_936+108insAC
NM_000539.3:c.936+107_936+108insAC MANE Select NP_000530.1:n.936+107_936+108insAC