Canonical Allele Identifier: CA601771375

Gene: DRD2

Linked Data

• dbSNP Id: rs1286585471
• gnomAD v2: 11-113346208-G-T
• gnomAD v3: 11-113475486-G-T
• gnomAD v4: 11-113475486-G-T
• MyVariant Identifiers: chr11:g.113346208G>T (hg19) ; chr11:g.113346208_113346209delinsTC (hg19) ; chr11:g.113475486G>T (hg38) ; chr11:g.113475486_113475487delinsTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475486G>T , CM000673.2:g.113475486G>T	GRCh38
NC_000011.9:g.113346208G>T , CM000673.1:g.113346208G>T	GRCh37
NC_000011.8:g.112851418G>T	NCBI36
NG_008841.1:g.4794C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000540600.5:n.34+172C>A