Canonical Allele Identifier: CA2758363913
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530775del , CM000665.2:g.129530775del GRCh38
NC_000003.11:g.129249618del , CM000665.1:g.129249618del GRCh37
NC_000003.10:g.130732308del NCBI36
NG_009115.1:g.7137del

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-101del MANE Select ENSP00000296271.3:n.362-101del
ENST00000296271.3:c.362-101del ENSP00000296271.3:n.362-101del
NM_000539.3:c.362-101del MANE Select NP_000530.1:n.362-101del