Canonical Allele Identifier: CA2001169023

Gene: DRD2

Linked Data

• dbSNP Id: rs1950810199

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414900T>C , CM000673.2:g.113414900T>C	GRCh38
NC_000011.9:g.113285622T>C , CM000673.1:g.113285622T>C	GRCh37
NC_000011.8:g.112790832T>C	NCBI36
NG_008841.1:g.65380A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.724-439A>G MANE Select	ENSP00000354859.3:n.724-439A>G
ENST00000346454.7:c.723+521A>G	ENSP00000278597.5:n.723+521A>G
ENST00000362072.7:c.724-439A>G	ENSP00000354859.3:n.724-439A>G
ENST00000535984.1:n.443-439A>G
ENST00000538967.5:c.724-439A>G	ENSP00000438215.1:n.724-439A>G
ENST00000540600.5:n.789-439A>G
ENST00000542968.5:c.724-439A>G	ENSP00000442172.1:n.724-439A>G
ENST00000544518.5:c.721-439A>G	ENSP00000441068.1:n.721-439A>G
NM_000795.3:c.724-439A>G	NP_000786.1:n.724-439A>G
NM_016574.3:c.723+521A>G	NP_057658.2:n.723+521A>G
XM_017017296.2:c.724-439A>G	XP_016872785.1:n.724-439A>G
NM_000795.4:c.724-439A>G MANE Select	NP_000786.1:n.724-439A>G
NM_016574.4:c.723+521A>G	NP_057658.2:n.723+521A>G