Canonical Allele Identifier: CA382648982

Gene: DRD2

Linked Data

• dbSNP Id: rs1195929717
• gnomAD v2: 11-113281480-C-T
• gnomAD v4: 11-113410758-C-T
• MyVariant Identifiers: chr11:g.113281480C>T (hg19) ; chr11:g.113410758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410758C>T , CM000673.2:g.113410758C>T	GRCh38
NC_000011.9:g.113281480C>T , CM000673.1:g.113281480C>T	GRCh37
NC_000011.8:g.112786690C>T	NCBI36
NG_008841.1:g.69522G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1301G>A MANE Select	ENSP00000354859.3:p.Arg434His
ENST00000346454.7:c.1214G>A	ENSP00000278597.5:p.Arg405His
ENST00000362072.7:c.1301G>A	ENSP00000354859.3:p.Arg434His
ENST00000538967.5:c.1307G>A	ENSP00000438215.1:p.Arg436His
ENST00000542968.5:c.1301G>A	ENSP00000442172.1:p.Arg434His
ENST00000544518.5:c.1298G>A	ENSP00000441068.1:p.Arg433His
NM_000795.3:c.1301G>A	NP_000786.1:p.Arg434His
NM_016574.3:c.1214G>A	NP_057658.2:p.Arg405His
XM_017017296.2:c.1301G>A	XP_016872785.1:p.Arg434His
NM_000795.4:c.1301G>A MANE Select	NP_000786.1:p.Arg434His
NM_016574.4:c.1214G>A	NP_057658.2:p.Arg405His