Canonical Allele Identifier: CA2758363911
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530761_129530762del , CM000665.2:g.129530761_129530762del GRCh38
NC_000003.11:g.129249604_129249605del , CM000665.1:g.129249604_129249605del GRCh37
NC_000003.10:g.130732294_130732295del NCBI36
NG_009115.1:g.7123_7124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-115_362-114del MANE Select ENSP00000296271.3:n.362-115_362-114del
ENST00000296271.3:c.362-115_362-114del ENSP00000296271.3:n.362-115_362-114del
NM_000539.3:c.362-115_362-114del MANE Select NP_000530.1:n.362-115_362-114del