Canonical Allele Identifier: CA2577961739

Gene: RHO

Linked Data

• gnomAD v4: 3-129530799-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530803_129530804dup , CM000665.2:g.129530803_129530804dup	GRCh38
NC_000003.11:g.129249646_129249647dup , CM000665.1:g.129249646_129249647dup	GRCh37
NC_000003.10:g.130732336_130732337dup	NCBI36
NG_009115.1:g.7165_7166dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.362-73_362-72dup MANE Select	ENSP00000296271.3:n.362-73_362-72dup
ENST00000296271.3:c.362-73_362-72dup	ENSP00000296271.3:n.362-73_362-72dup
NM_000539.3:c.362-73_362-72dup MANE Select	NP_000530.1:n.362-73_362-72dup