Canonical Allele Identifier: CA228626140

Gene: DRD2

Linked Data

• dbSNP Id: rs112788137
• MyVariant Identifiers: chr11:g.113285463T>C (hg19) ; chr11:g.113414741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414741T>C , CM000673.2:g.113414741T>C	GRCh38
NC_000011.9:g.113285463T>C , CM000673.1:g.113285463T>C	GRCh37
NC_000011.8:g.112790673T>C	NCBI36
NG_008841.1:g.65539A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-280A>G MANE Select	ENSP00000354859.3:n.724-280A>G
ENST00000346454.7:c.723+680A>G	ENSP00000278597.5:n.723+680A>G
ENST00000362072.7:c.724-280A>G	ENSP00000354859.3:n.724-280A>G
ENST00000535984.1:n.443-280A>G
ENST00000538967.5:c.724-280A>G	ENSP00000438215.1:n.724-280A>G
ENST00000540600.5:n.789-280A>G
ENST00000542968.5:c.724-280A>G	ENSP00000442172.1:n.724-280A>G
ENST00000544518.5:c.721-280A>G	ENSP00000441068.1:n.721-280A>G
NM_000795.3:c.724-280A>G	NP_000786.1:n.724-280A>G
NM_016574.3:c.723+680A>G	NP_057658.2:n.723+680A>G
XM_017017296.2:c.724-280A>G	XP_016872785.1:n.724-280A>G
NM_000795.4:c.724-280A>G MANE Select	NP_000786.1:n.724-280A>G
NM_016574.4:c.723+680A>G	NP_057658.2:n.723+680A>G