Canonical Allele Identifier: CA477043221

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283492G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412770G>T , CM000673.2:g.113412770G>T	GRCh38
NC_000011.9:g.113283492G>T , CM000673.1:g.113283492G>T	GRCh37
NC_000011.8:g.112788702G>T	NCBI36
NG_008841.1:g.67510C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.924C>A MANE Select	ENSP00000354859.3:p.Pro308=
ENST00000346454.7:c.837C>A	ENSP00000278597.5:p.Pro279=
ENST00000362072.7:c.924C>A	ENSP00000354859.3:p.Pro308=
ENST00000538967.5:c.930C>A	ENSP00000438215.1:p.Pro310=
ENST00000542968.5:c.924C>A	ENSP00000442172.1:p.Pro308=
ENST00000544518.5:c.921C>A	ENSP00000441068.1:p.Pro307=
NM_000795.3:c.924C>A	NP_000786.1:p.Pro308=
NM_016574.3:c.837C>A	NP_057658.2:p.Pro279=
XM_017017296.2:c.924C>A	XP_016872785.1:p.Pro308=
NM_000795.4:c.924C>A MANE Select	NP_000786.1:p.Pro308=
NM_016574.4:c.837C>A	NP_057658.2:p.Pro279=