Canonical Allele Identifier: CA671861428

Gene: DRD2

Linked Data

• dbSNP Id: rs1279900612
• gnomAD v3: 11-113475392-C-T
• gnomAD v4: 11-113475392-C-T
• MyVariant Identifiers: chr11:g.113346114C>T (hg19) ; chr11:g.113475392C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113475392C>T , CM000673.2:g.113475392C>T	GRCh38
NC_000011.9:g.113346114C>T , CM000673.1:g.113346114C>T	GRCh37
NC_000011.8:g.112851324C>T	NCBI36
NG_008841.1:g.4888G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-348G>A MANE Select	ENSP00000354859.3:n.-348G>A
ENST00000540600.5:n.34+266G>A
NM_000795.4:c.-348G>A MANE Select	NP_000786.1:n.-348G>A
NM_016574.4:c.-348G>A	NP_057658.2:n.-348G>A