Canonical Allele Identifier: CA2001183715

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113464537A= , CM000673.2:g.113464537A=	GRCh38
NC_000011.9:g.113335259A= , CM000673.1:g.113335259A=	GRCh37
NC_000011.8:g.112840469A=	NCBI36
NG_008841.1:g.15743T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000795.4:c.-32+10539T= MANE Select	NP_000786.1:n.-32+10539T=
ENST00000362072.8:c.-32+10539T= MANE Select	ENSP00000354859.3:n.-32+10539T=
NM_000795.3:c.-32+10539T=	NP_000786.1:n.-32+10539T=
NM_016574.3:c.-32+10539T=	NP_057658.2:n.-32+10539T=
NM_016574.4:c.-32+10539T=	NP_057658.2:n.-32+10539T=
ENST00000346454.7:c.-32+10539T=	ENSP00000278597.5:n.-32+10539T=
ENST00000362072.7:c.-32+10539T=	ENSP00000354859.3:n.-32+10539T=
ENST00000540600.5:n.34+11121T=
ENST00000542616.1:c.-32+9693T=	ENSP00000441474.1:n.-32+9693T=
XM_017017296.2:c.-32+9693T=	XP_016872785.1:n.-32+9693T=