Canonical Allele Identifier: CA1401210826
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084785426

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532244T>C , CM000665.2:g.129532244T>C GRCh38
NC_000003.11:g.129251087T>C , CM000665.1:g.129251087T>C GRCh37
NC_000003.10:g.130733777T>C NCBI36
NG_009115.1:g.8606T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-7T>C MANE Select ENSP00000296271.3:n.531-7T>C
ENST00000296271.3:c.531-7T>C ENSP00000296271.3:n.531-7T>C
NM_000539.3:c.531-7T>C MANE Select NP_000530.1:n.531-7T>C