Canonical Allele Identifier: CA2667616070
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530807_129530811del , CM000665.2:g.129530807_129530811del GRCh38
NC_000003.11:g.129249650_129249654del , CM000665.1:g.129249650_129249654del GRCh37
NC_000003.10:g.130732340_130732344del NCBI36
NG_009115.1:g.7169_7173del

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-69_362-65del MANE Select ENSP00000296271.3:n.362-69_362-65del
ENST00000296271.3:c.362-69_362-65del ENSP00000296271.3:n.362-69_362-65del
NM_000539.3:c.362-69_362-65del MANE Select NP_000530.1:n.362-69_362-65del