Canonical Allele Identifier: CA898754710
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs867005068

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533722C>T , CM000665.2:g.129533722C>T GRCh38
NC_000003.11:g.129252565C>T , CM000665.1:g.129252565C>T GRCh37
NC_000003.10:g.130735255C>T NCBI36
NG_009115.1:g.10084C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.*4C>T MANE Select ENSP00000296271.3:n.*4C>T
ENST00000296271.3:c.*4C>T ENSP00000296271.3:n.*4C>T
NM_000539.3:c.*4C>T MANE Select NP_000530.1:n.*4C>T