Canonical Allele Identifier: CA1401212303
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532880C= , CM000665.2:g.129532880C= GRCh38
NC_000003.11:g.129251723C= , CM000665.1:g.129251723C= GRCh37
NC_000003.10:g.130734413C= NCBI36
NG_009115.1:g.9242C=

Transcript Alleles

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