Canonical Allele Identifier: CA354498463
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2108749972

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530987C>T , CM000665.2:g.129530987C>T GRCh38
NC_000003.11:g.129249830C>T , CM000665.1:g.129249830C>T GRCh37
NC_000003.10:g.130732520C>T NCBI36
NG_009115.1:g.7349C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.473C>T MANE Select ENSP00000296271.3:p.Ala158Val
ENST00000296271.3:c.473C>T ENSP00000296271.3:p.Ala158Val
NM_000539.3:c.473C>T MANE Select NP_000530.1:p.Ala158Val