Canonical Allele Identifier: CA1401208193
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084770823

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530524_129530528del , CM000665.2:g.129530524_129530528del GRCh38
NC_000003.11:g.129249367_129249371del , CM000665.1:g.129249367_129249371del GRCh37
NC_000003.10:g.130732057_130732061del NCBI36
NG_009115.1:g.6886_6890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-352_362-348del MANE Select ENSP00000296271.3:n.362-352_362-348del
ENST00000296271.3:c.362-352_362-348del ENSP00000296271.3:n.362-352_362-348del
NM_000539.3:c.362-352_362-348del MANE Select NP_000530.1:n.362-352_362-348del