Canonical Allele Identifier: CA898751400

Gene: RHO

Linked Data

• dbSNP Id: rs1553781099
• gnomAD v3: 3-129530533-A-ACAACACACACACAC
• gnomAD v4: 3-129530533-A-ACAACACACACACAC
• MyVariant Identifiers: chr3:g.129249376_129249377insCAACACACACACAC (hg19) ; chr3:g.129530533_129530534insCAACACACACACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530533_129530534insCAACACACACACAC , CM000665.2:g.129530533_129530534insCAACACACACACAC	GRCh38
NC_000003.11:g.129249376_129249377insCAACACACACACAC , CM000665.1:g.129249376_129249377insCAACACACACACAC	GRCh37
NC_000003.10:g.130732066_130732067insCAACACACACACAC	NCBI36
NG_009115.1:g.6895_6896insCAACACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.362-343_362-342insCAACACACACACAC MANE Select	ENSP00000296271.3:n.362-343_362-342insCAACACACACACAC
ENST00000296271.3:c.362-343_362-342insCAACACACACACAC	ENSP00000296271.3:n.362-343_362-342insCAACACACACACAC
NM_000539.3:c.362-343_362-342insCAACACACACACAC MANE Select	NP_000530.1:n.362-343_362-342insCAACACACACACAC