Canonical Allele Identifier: CA382650200

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283464T>A (hg19) ; chr11:g.113412742T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412742T>A , CM000673.2:g.113412742T>A	GRCh38
NC_000011.9:g.113283464T>A , CM000673.1:g.113283464T>A	GRCh37
NC_000011.8:g.112788674T>A	NCBI36
NG_008841.1:g.67538A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.952A>T MANE Select	ENSP00000354859.3:p.Thr318Ser
ENST00000346454.7:c.865A>T	ENSP00000278597.5:p.Thr289Ser
ENST00000362072.7:c.952A>T	ENSP00000354859.3:p.Thr318Ser
ENST00000538967.5:c.958A>T	ENSP00000438215.1:p.Thr320Ser
ENST00000542968.5:c.952A>T	ENSP00000442172.1:p.Thr318Ser
ENST00000544518.5:c.949A>T	ENSP00000441068.1:p.Thr317Ser
NM_000795.3:c.952A>T	NP_000786.1:p.Thr318Ser
NM_016574.3:c.865A>T	NP_057658.2:p.Thr289Ser
XM_017017296.2:c.952A>T	XP_016872785.1:p.Thr318Ser
NM_000795.4:c.952A>T MANE Select	NP_000786.1:p.Thr318Ser
NM_016574.4:c.865A>T	NP_057658.2:p.Thr289Ser