Canonical Allele Identifier: CA354495454
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1451320951

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528794C>T , CM000665.2:g.129528794C>T GRCh38
NC_000003.11:g.129247637C>T , CM000665.1:g.129247637C>T GRCh37
NC_000003.10:g.130730327C>T NCBI36
NG_009115.1:g.5156C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.61C>T MANE Select ENSP00000296271.3:p.Arg21Cys
ENST00000296271.3:c.61C>T ENSP00000296271.3:p.Arg21Cys
NM_000539.3:c.61C>T MANE Select NP_000530.1:p.Arg21Cys