Canonical Allele Identifier: CA2758363882
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530534_129530548del , CM000665.2:g.129530534_129530548del GRCh38
NC_000003.11:g.129249377_129249391del , CM000665.1:g.129249377_129249391del GRCh37
NC_000003.10:g.130732067_130732081del NCBI36
NG_009115.1:g.6896_6910del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-342_362-328del MANE Select ENSP00000296271.3:n.362-342_362-328del
ENST00000296271.3:c.362-342_362-328del ENSP00000296271.3:n.362-342_362-328del
NM_000539.3:c.362-342_362-328del MANE Select NP_000530.1:n.362-342_362-328del