Canonical Allele Identifier: CA2667616032
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530764dup , CM000665.2:g.129530764dup GRCh38
NC_000003.11:g.129249607dup , CM000665.1:g.129249607dup GRCh37
NC_000003.10:g.130732297dup NCBI36
NG_009115.1:g.7126dup

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-112dup MANE Select ENSP00000296271.3:n.362-112dup
ENST00000296271.3:c.362-112dup ENSP00000296271.3:n.362-112dup
NM_000539.3:c.362-112dup MANE Select NP_000530.1:n.362-112dup