Canonical Allele Identifier: CA6281204

Gene: DRD2

Linked Data

• dbSNP Id: rs766300123
• ExAC: 11:113283362 G / A
• gnomAD v2: 11-113283362-G-A
• gnomAD v3: 11-113412640-G-A
• gnomAD v4: 11-113412640-G-A
• MyVariant Identifiers: chr11:g.113283362G>A (hg19) ; chr11:g.113412640G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412640G>A , CM000673.2:g.113412640G>A	GRCh38
NC_000011.9:g.113283362G>A , CM000673.1:g.113283362G>A	GRCh37
NC_000011.8:g.112788572G>A	NCBI36
NG_008841.1:g.67640C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1054C>T MANE Select	ENSP00000354859.3:p.Arg352Trp
ENST00000346454.7:c.967C>T	ENSP00000278597.5:p.Arg323Trp
ENST00000362072.7:c.1054C>T	ENSP00000354859.3:p.Arg352Trp
ENST00000538967.5:c.1060C>T	ENSP00000438215.1:p.Arg354Trp
ENST00000542968.5:c.1054C>T	ENSP00000442172.1:p.Arg352Trp
ENST00000544518.5:c.1051C>T	ENSP00000441068.1:p.Arg351Trp
NM_000795.3:c.1054C>T	NP_000786.1:p.Arg352Trp
NM_016574.3:c.967C>T	NP_057658.2:p.Arg323Trp
XM_017017296.2:c.1054C>T	XP_016872785.1:p.Arg352Trp
NM_000795.4:c.1054C>T MANE Select	NP_000786.1:p.Arg352Trp
NM_016574.4:c.967C>T	NP_057658.2:p.Arg323Trp