Canonical Allele Identifier: CA2758363918
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530821dup , CM000665.2:g.129530821dup GRCh38
NC_000003.11:g.129249664dup , CM000665.1:g.129249664dup GRCh37
NC_000003.10:g.130732354dup NCBI36
NG_009115.1:g.7183dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-55dup MANE Select ENSP00000296271.3:n.362-55dup
ENST00000296271.3:c.362-55dup ENSP00000296271.3:n.362-55dup
NM_000539.3:c.362-55dup MANE Select NP_000530.1:n.362-55dup