Canonical Allele Identifier: CA382650081

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283434T>G (hg19) ; chr11:g.113412712T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412712T>G , CM000673.2:g.113412712T>G	GRCh38
NC_000011.9:g.113283434T>G , CM000673.1:g.113283434T>G	GRCh37
NC_000011.8:g.112788644T>G	NCBI36
NG_008841.1:g.67568A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.982A>C MANE Select	ENSP00000354859.3:p.Asn328His
ENST00000346454.7:c.895A>C	ENSP00000278597.5:p.Asn299His
ENST00000362072.7:c.982A>C	ENSP00000354859.3:p.Asn328His
ENST00000538967.5:c.988A>C	ENSP00000438215.1:p.Asn330His
ENST00000542968.5:c.982A>C	ENSP00000442172.1:p.Asn328His
ENST00000544518.5:c.979A>C	ENSP00000441068.1:p.Asn327His
NM_000795.3:c.982A>C	NP_000786.1:p.Asn328His
NM_016574.3:c.895A>C	NP_057658.2:p.Asn299His
XM_017017296.2:c.982A>C	XP_016872785.1:p.Asn328His
NM_000795.4:c.982A>C MANE Select	NP_000786.1:p.Asn328His
NM_016574.4:c.895A>C	NP_057658.2:p.Asn299His