Canonical Allele Identifier: CA6281149

Gene: DRD2

Linked Data

• dbSNP Id: rs778778364
• ExAC: 11:113281527 G / A
• gnomAD v4: 11-113410805-G-A
• MyVariant Identifiers: chr11:g.113281527G>A (hg19) ; chr11:g.113410805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410805G>A , CM000673.2:g.113410805G>A	GRCh38
NC_000011.9:g.113281527G>A , CM000673.1:g.113281527G>A	GRCh37
NC_000011.8:g.112786737G>A	NCBI36
NG_008841.1:g.69475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1254C>T MANE Select	ENSP00000354859.3:p.Asn418=
ENST00000346454.7:c.1167C>T	ENSP00000278597.5:p.Asn389=
ENST00000362072.7:c.1254C>T	ENSP00000354859.3:p.Asn418=
ENST00000538967.5:c.1260C>T	ENSP00000438215.1:p.Asn420=
ENST00000542968.5:c.1254C>T	ENSP00000442172.1:p.Asn418=
ENST00000544518.5:c.1251C>T	ENSP00000441068.1:p.Asn417=
NM_000795.3:c.1254C>T	NP_000786.1:p.Asn418=
NM_016574.3:c.1167C>T	NP_057658.2:p.Asn389=
XM_017017296.2:c.1254C>T	XP_016872785.1:p.Asn418=
NM_000795.4:c.1254C>T MANE Select	NP_000786.1:p.Asn418=
NM_016574.4:c.1167C>T	NP_057658.2:p.Asn389=