Canonical Allele Identifier: CA1401210491
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531834T= , CM000665.2:g.129531834T= GRCh38
NC_000003.11:g.129250677T= , CM000665.1:g.129250677T= GRCh37
NC_000003.10:g.130733367T= NCBI36
NG_009115.1:g.8196T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-417T= MANE Select ENSP00000296271.3:n.531-417T=
ENST00000296271.3:c.531-417T= ENSP00000296271.3:n.531-417T=
NM_000539.3:c.531-417T= MANE Select NP_000530.1:n.531-417T=