Canonical Allele Identifier: CA2001166998

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410498G= , CM000673.2:g.113410498G=	GRCh38
NC_000011.9:g.113281220G= , CM000673.1:g.113281220G=	GRCh37
NC_000011.8:g.112786430G=	NCBI36
NG_008841.1:g.69782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.*229C= MANE Select	ENSP00000354859.3:n.*229C=
ENST00000346454.7:c.*229C=	ENSP00000278597.5:n.*229C=
ENST00000362072.7:c.*229C=	ENSP00000354859.3:n.*229C=
ENST00000542968.5:c.*229C=	ENSP00000442172.1:n.*229C=
ENST00000544518.5:c.*229C=	ENSP00000441068.1:n.*229C=
NM_000795.3:c.*229C=	NP_000786.1:n.*229C=
NM_016574.3:c.*229C=	NP_057658.2:n.*229C=
XM_017017296.2:c.*229C=	XP_016872785.1:n.*229C=
NM_000795.4:c.*229C= MANE Select	NP_000786.1:n.*229C=
NM_016574.4:c.*229C=	NP_057658.2:n.*229C=