Canonical Allele Identifier: CA382650043

Gene: DRD2

Linked Data

• dbSNP Id: rs1479691191
• gnomAD v2: 11-113283425-C-T
• gnomAD v3: 11-113412703-C-T
• gnomAD v4: 11-113412703-C-T
• MyVariant Identifiers: chr11:g.113283425C>T (hg19) ; chr11:g.113412703C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412703C>T , CM000673.2:g.113412703C>T	GRCh38
NC_000011.9:g.113283425C>T , CM000673.1:g.113283425C>T	GRCh37
NC_000011.8:g.112788635C>T	NCBI36
NG_008841.1:g.67577G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.991G>A MANE Select	ENSP00000354859.3:p.Ala331Thr
ENST00000346454.7:c.904G>A	ENSP00000278597.5:p.Ala302Thr
ENST00000362072.7:c.991G>A	ENSP00000354859.3:p.Ala331Thr
ENST00000538967.5:c.997G>A	ENSP00000438215.1:p.Ala333Thr
ENST00000542968.5:c.991G>A	ENSP00000442172.1:p.Ala331Thr
ENST00000544518.5:c.988G>A	ENSP00000441068.1:p.Ala330Thr
NM_000795.3:c.991G>A	NP_000786.1:p.Ala331Thr
NM_016574.3:c.904G>A	NP_057658.2:p.Ala302Thr
XM_017017296.2:c.991G>A	XP_016872785.1:p.Ala331Thr
NM_000795.4:c.991G>A MANE Select	NP_000786.1:p.Ala331Thr
NM_016574.4:c.904G>A	NP_057658.2:p.Ala302Thr