Canonical Allele Identifier: CA671868381

Gene: DRD2

Linked Data

• dbSNP Id: rs2734839
• MyVariant Identifiers: chr11:g.113286490C>A (hg19) ; chr11:g.113415768C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113415768C>A , CM000673.2:g.113415768C>A	GRCh38
NC_000011.9:g.113286490C>A , CM000673.1:g.113286490C>A	GRCh37
NC_000011.8:g.112791700C>A	NCBI36
NG_008841.1:g.64512G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.533-157G>T MANE Select	ENSP00000354859.3:n.533-157G>T
ENST00000346454.7:c.533-157G>T	ENSP00000278597.5:n.533-157G>T
ENST00000362072.7:c.533-157G>T	ENSP00000354859.3:n.533-157G>T
ENST00000535984.1:n.252-157G>T
ENST00000538967.5:c.533-157G>T	ENSP00000438215.1:n.533-157G>T
ENST00000539420.1:n.229-157G>T
ENST00000540600.5:n.598-157G>T
ENST00000542968.5:c.533-157G>T	ENSP00000442172.1:n.533-157G>T
ENST00000544518.5:c.530-157G>T	ENSP00000441068.1:n.530-157G>T
NM_000795.3:c.533-157G>T	NP_000786.1:n.533-157G>T
NM_016574.3:c.533-157G>T	NP_057658.2:n.533-157G>T
XM_017017296.2:c.533-157G>T	XP_016872785.1:n.533-157G>T
NM_000795.4:c.533-157G>T MANE Select	NP_000786.1:n.533-157G>T
NM_016574.4:c.533-157G>T	NP_057658.2:n.533-157G>T