Canonical Allele Identifier: CA354498373
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530975T>C , CM000665.2:g.129530975T>C GRCh38
NC_000003.11:g.129249818T>C , CM000665.1:g.129249818T>C GRCh37
NC_000003.10:g.130732508T>C NCBI36
NG_009115.1:g.7337T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.461T>C MANE Select ENSP00000296271.3:p.Ile154Thr
ENST00000296271.3:c.461T>C ENSP00000296271.3:p.Ile154Thr
NM_000539.3:c.461T>C MANE Select NP_000530.1:p.Ile154Thr