Canonical Allele Identifier: CA354497927
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530892G>T , CM000665.2:g.129530892G>T GRCh38
NC_000003.11:g.129249735G>T , CM000665.1:g.129249735G>T GRCh37
NC_000003.10:g.130732425G>T NCBI36
NG_009115.1:g.7254G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.378G>T MANE Select ENSP00000296271.3:p.Trp126Cys
ENST00000296271.3:c.378G>T ENSP00000296271.3:p.Trp126Cys
NM_000539.3:c.378G>T MANE Select NP_000530.1:p.Trp126Cys