Canonical Allele Identifier: CA228626161

Gene: DRD2

Linked Data

• dbSNP Id: rs887781497
• gnomAD v3: 11-113414865-C-T
• gnomAD v4: 11-113414865-C-T
• MyVariant Identifiers: chr11:g.113285587C>T (hg19) ; chr11:g.113414865C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414865C>T , CM000673.2:g.113414865C>T	GRCh38
NC_000011.9:g.113285587C>T , CM000673.1:g.113285587C>T	GRCh37
NC_000011.8:g.112790797C>T	NCBI36
NG_008841.1:g.65415G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-404G>A MANE Select	ENSP00000354859.3:n.724-404G>A
ENST00000346454.7:c.723+556G>A	ENSP00000278597.5:n.723+556G>A
ENST00000362072.7:c.724-404G>A	ENSP00000354859.3:n.724-404G>A
ENST00000535984.1:n.443-404G>A
ENST00000538967.5:c.724-404G>A	ENSP00000438215.1:n.724-404G>A
ENST00000540600.5:n.789-404G>A
ENST00000542968.5:c.724-404G>A	ENSP00000442172.1:n.724-404G>A
ENST00000544518.5:c.721-404G>A	ENSP00000441068.1:n.721-404G>A
NM_000795.3:c.724-404G>A	NP_000786.1:n.724-404G>A
NM_016574.3:c.723+556G>A	NP_057658.2:n.723+556G>A
XM_017017296.2:c.724-404G>A	XP_016872785.1:n.724-404G>A
NM_000795.4:c.724-404G>A MANE Select	NP_000786.1:n.724-404G>A
NM_016574.4:c.723+556G>A	NP_057658.2:n.723+556G>A