Canonical Allele Identifier: CA354496448
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528971G>A , CM000665.2:g.129528971G>A GRCh38
NC_000003.11:g.129247814G>A , CM000665.1:g.129247814G>A GRCh37
NC_000003.10:g.130730504G>A NCBI36
NG_009115.1:g.5333G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.238G>A MANE Select ENSP00000296271.3:p.Ala80Thr
ENST00000296271.3:c.238G>A ENSP00000296271.3:p.Ala80Thr
NM_000539.3:c.238G>A MANE Select NP_000530.1:p.Ala80Thr