Canonical Allele Identifier: CA2001161788

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442537A= , CM000673.2:g.113442537A=	GRCh38
NC_000011.9:g.113313259A= , CM000673.1:g.113313259A=	GRCh37
NC_000011.8:g.112818469A=	NCBI36
NG_008841.1:g.37743T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-17855T= MANE Select	ENSP00000354859.3:n.-31-17855T=
ENST00000346454.7:c.-31-17855T=	ENSP00000278597.5:n.-31-17855T=
ENST00000362072.7:c.-31-17855T=	ENSP00000354859.3:n.-31-17855T=
ENST00000540600.5:n.35-17855T=
ENST00000542616.1:c.-31-17855T=	ENSP00000441474.1:n.-31-17855T=
ENST00000543292.1:c.-32+5034T=	ENSP00000438419.1:n.-32+5034T=
NM_000795.3:c.-31-17855T=	NP_000786.1:n.-31-17855T=
NM_016574.3:c.-31-17855T=	NP_057658.2:n.-31-17855T=
XM_017017296.2:c.-31-17855T=	XP_016872785.1:n.-31-17855T=
NM_000795.4:c.-31-17855T= MANE Select	NP_000786.1:n.-31-17855T=
NM_016574.4:c.-31-17855T=	NP_057658.2:n.-31-17855T=