Allele Registry

Canonical Allele Identifier: CA228631686

Gene: DRD2 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.113475529_113475530insG

GRCh37 chr11:g.113346251_113346252insG

Linked Data - Sequence & Population

gnomAD v2:

11:113346251 T / TG

gnomAD v3:

11:113475529 T / TG

gnomAD v4:

chr11-113475529-T-TG

Joint Max Group AF 0.89719148 (NFE)

Genomes Max Group AF 0.89723089 (NFE)

Exomes Max Group AF 0.51841371 (NFE)

Linked Data - NCBI & NCI

ClinVar Allele:

1228219

ClinVar RCV:

RCV001638497

RCV002072946

ClinVar Variation:

1236510

dbSNP:

1799732

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475530dup , CM000673.2:g.113475530dup	GRCh38
NC_000011.9:g.113346252dup , CM000673.1:g.113346252dup	GRCh37
NC_000011.8:g.112851462dup	NCBI36
NG_008841.1:g.4750dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540600.5:n.34+128dup
XR_948024.2:n.912dup

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