Canonical Allele Identifier: CA228631681

Gene: DRD2

Linked Data

• dbSNP Id: rs541279241
• gnomAD v2: 11-113346219-A-T
• gnomAD v3: 11-113475497-A-T
• gnomAD v4: 11-113475497-A-T
• MyVariant Identifiers: chr11:g.113346219A>T (hg19) ; chr11:g.113475497A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475497A>T , CM000673.2:g.113475497A>T	GRCh38
NC_000011.9:g.113346219A>T , CM000673.1:g.113346219A>T	GRCh37
NC_000011.8:g.112851429A>T	NCBI36
NG_008841.1:g.4783T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540600.5:n.34+161T>A