Canonical Allele Identifier: CA942361575

Gene: DRD2

Linked Data

• dbSNP Id: rs1950820162
• gnomAD v3: 11-113415800-A-C
• gnomAD v4: 11-113415800-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113415800A>C , CM000673.2:g.113415800A>C	GRCh38
NC_000011.9:g.113286522A>C , CM000673.1:g.113286522A>C	GRCh37
NC_000011.8:g.112791732A>C	NCBI36
NG_008841.1:g.64480T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.533-189T>G MANE Select	ENSP00000354859.3:n.533-189T>G
ENST00000346454.7:c.533-189T>G	ENSP00000278597.5:n.533-189T>G
ENST00000362072.7:c.533-189T>G	ENSP00000354859.3:n.533-189T>G
ENST00000535984.1:n.252-189T>G
ENST00000538967.5:c.533-189T>G	ENSP00000438215.1:n.533-189T>G
ENST00000539420.1:n.229-189T>G
ENST00000540600.5:n.598-189T>G
ENST00000542968.5:c.533-189T>G	ENSP00000442172.1:n.533-189T>G
ENST00000544518.5:c.530-189T>G	ENSP00000441068.1:n.530-189T>G
NM_000795.3:c.533-189T>G	NP_000786.1:n.533-189T>G
NM_016574.3:c.533-189T>G	NP_057658.2:n.533-189T>G
XM_017017296.2:c.533-189T>G	XP_016872785.1:n.533-189T>G
NM_000795.4:c.533-189T>G MANE Select	NP_000786.1:n.533-189T>G
NM_016574.4:c.533-189T>G	NP_057658.2:n.533-189T>G