Canonical Allele Identifier: CA601771383

Gene: DRD2

Linked Data

• dbSNP Id: rs1345123024
• gnomAD v2: 11-113346266-G-C
• gnomAD v3: 11-113475544-G-C
• gnomAD v4: 11-113475544-G-C
• MyVariant Identifiers: chr11:g.113346266G>C (hg19) ; chr11:g.113475544G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475544G>C , CM000673.2:g.113475544G>C	GRCh38
NC_000011.9:g.113346266G>C , CM000673.1:g.113346266G>C	GRCh37
NC_000011.8:g.112851476G>C	NCBI36
NG_008841.1:g.4736C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000540600.5:n.34+114C>G
XR_948024.2:n.898C>G