Canonical Allele Identifier: CA354496663
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529007A>T , CM000665.2:g.129529007A>T GRCh38
NC_000003.11:g.129247850A>T , CM000665.1:g.129247850A>T GRCh37
NC_000003.10:g.130730540A>T NCBI36
NG_009115.1:g.5369A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.274A>T MANE Select ENSP00000296271.3:p.Thr92Ser
ENST00000296271.3:c.274A>T ENSP00000296271.3:p.Thr92Ser
NM_000539.3:c.274A>T MANE Select NP_000530.1:p.Thr92Ser