Canonical Allele Identifier: CA1401208164
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530518C= , CM000665.2:g.129530518C= GRCh38
NC_000003.11:g.129249361C= , CM000665.1:g.129249361C= GRCh37
NC_000003.10:g.130732051C= NCBI36
NG_009115.1:g.6880C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-358C= MANE Select ENSP00000296271.3:n.362-358C=
ENST00000296271.3:c.362-358C= ENSP00000296271.3:n.362-358C=
NM_000539.3:c.362-358C= MANE Select NP_000530.1:n.362-358C=