Canonical Allele Identifier: CA2001167132

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410734T= , CM000673.2:g.113410734T=	GRCh38
NC_000011.9:g.113281456T= , CM000673.1:g.113281456T=	GRCh37
NC_000011.8:g.112786666T=	NCBI36
NG_008841.1:g.69546A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1325A= MANE Select	ENSP00000354859.3:p.His442=
ENST00000346454.7:c.1238A=	ENSP00000278597.5:p.His413=
ENST00000362072.7:c.1325A=	ENSP00000354859.3:p.His442=
ENST00000538967.5:c.1331A=	ENSP00000438215.1:p.His444=
ENST00000542968.5:c.1325A=	ENSP00000442172.1:p.His442=
ENST00000544518.5:c.1322A=	ENSP00000441068.1:p.His441=
NM_000795.3:c.1325A=	NP_000786.1:p.His442=
NM_016574.3:c.1238A=	NP_057658.2:p.His413=
XM_017017296.2:c.1325A=	XP_016872785.1:p.His442=
NM_000795.4:c.1325A= MANE Select	NP_000786.1:p.His442=
NM_016574.4:c.1238A=	NP_057658.2:p.His413=