Canonical Allele Identifier: CA382648928

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281455G>T (hg19) ; chr11:g.113410733G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410733G>T , CM000673.2:g.113410733G>T	GRCh38
NC_000011.9:g.113281455G>T , CM000673.1:g.113281455G>T	GRCh37
NC_000011.8:g.112786665G>T	NCBI36
NG_008841.1:g.69547C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1326C>A MANE Select	ENSP00000354859.3:p.His442Gln
ENST00000346454.7:c.1239C>A	ENSP00000278597.5:p.His413Gln
ENST00000362072.7:c.1326C>A	ENSP00000354859.3:p.His442Gln
ENST00000538967.5:c.1332C>A	ENSP00000438215.1:p.His444Gln
ENST00000542968.5:c.1326C>A	ENSP00000442172.1:p.His442Gln
ENST00000544518.5:c.1323C>A	ENSP00000441068.1:p.His441Gln
NM_000795.3:c.1326C>A	NP_000786.1:p.His442Gln
NM_016574.3:c.1239C>A	NP_057658.2:p.His413Gln
XM_017017296.2:c.1326C>A	XP_016872785.1:p.His442Gln
NM_000795.4:c.1326C>A MANE Select	NP_000786.1:p.His442Gln
NM_016574.4:c.1239C>A	NP_057658.2:p.His413Gln