Canonical Allele Identifier: CA2667616079
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530813_129530826del , CM000665.2:g.129530813_129530826del GRCh38
NC_000003.11:g.129249656_129249669del , CM000665.1:g.129249656_129249669del GRCh37
NC_000003.10:g.130732346_130732359del NCBI36
NG_009115.1:g.7175_7188del

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-63_362-50del MANE Select ENSP00000296271.3:n.362-63_362-50del
ENST00000296271.3:c.362-63_362-50del ENSP00000296271.3:n.362-63_362-50del
NM_000539.3:c.362-63_362-50del MANE Select NP_000530.1:n.362-63_362-50del