Canonical Allele Identifier: CA671861486

Gene: DRD2

Linked Data

• dbSNP Id: rs1285300068
• gnomAD v3: 11-113475458-C-G
• gnomAD v4: 11-113475458-C-G
• MyVariant Identifiers: chr11:g.113346180C>G (hg19) ; chr11:g.113475458C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475458C>G , CM000673.2:g.113475458C>G	GRCh38
NC_000011.9:g.113346180C>G , CM000673.1:g.113346180C>G	GRCh37
NC_000011.8:g.112851390C>G	NCBI36
NG_008841.1:g.4822G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000540600.5:n.34+200G>C