Canonical Allele Identifier: CA2001168016

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412777G= , CM000673.2:g.113412777G=	GRCh38
NC_000011.9:g.113283499G= , CM000673.1:g.113283499G=	GRCh37
NC_000011.8:g.112788709G=	NCBI36
NG_008841.1:g.67503C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.917C= MANE Select	ENSP00000354859.3:p.Thr306=
ENST00000346454.7:c.830C=	ENSP00000278597.5:p.Thr277=
ENST00000362072.7:c.917C=	ENSP00000354859.3:p.Thr306=
ENST00000538967.5:c.923C=	ENSP00000438215.1:p.Thr308=
ENST00000542968.5:c.917C=	ENSP00000442172.1:p.Thr306=
ENST00000544518.5:c.914C=	ENSP00000441068.1:p.Thr305=
NM_000795.3:c.917C=	NP_000786.1:p.Thr306=
NM_016574.3:c.830C=	NP_057658.2:p.Thr277=
XM_017017296.2:c.917C=	XP_016872785.1:p.Thr306=
NM_000795.4:c.917C= MANE Select	NP_000786.1:p.Thr306=
NM_016574.4:c.830C=	NP_057658.2:p.Thr277=