Canonical Allele Identifier: CA1401209116
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084774316

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530819A>G , CM000665.2:g.129530819A>G GRCh38
NC_000003.11:g.129249662A>G , CM000665.1:g.129249662A>G GRCh37
NC_000003.10:g.130732352A>G NCBI36
NG_009115.1:g.7181A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-57A>G MANE Select ENSP00000296271.3:n.362-57A>G
ENST00000296271.3:c.362-57A>G ENSP00000296271.3:n.362-57A>G
NM_000539.3:c.362-57A>G MANE Select NP_000530.1:n.362-57A>G