Canonical Allele Identifier: CA2001186461

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113470669T= , CM000673.2:g.113470669T=	GRCh38
NC_000011.9:g.113341391T= , CM000673.1:g.113341391T=	GRCh37
NC_000011.8:g.112846601T=	NCBI36
NG_008841.1:g.9611A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000795.4:c.-32+4407A= MANE Select	NP_000786.1:n.-32+4407A=
ENST00000362072.8:c.-32+4407A= MANE Select	ENSP00000354859.3:n.-32+4407A=
NM_000795.3:c.-32+4407A=	NP_000786.1:n.-32+4407A=
NM_016574.3:c.-32+4407A=	NP_057658.2:n.-32+4407A=
NM_016574.4:c.-32+4407A=	NP_057658.2:n.-32+4407A=
ENST00000346454.7:c.-32+4407A=	ENSP00000278597.5:n.-32+4407A=
ENST00000362072.7:c.-32+4407A=	ENSP00000354859.3:n.-32+4407A=
ENST00000540600.5:n.34+4989A=
ENST00000542616.1:c.-32+3561A=	ENSP00000441474.1:n.-32+3561A=
XM_017017296.2:c.-32+3561A=	XP_016872785.1:n.-32+3561A=