Canonical Allele Identifier: CA228626144

Gene: DRD2

Linked Data

• dbSNP Id: rs1015871636
• gnomAD v2: 11-113285508-A-G
• gnomAD v3: 11-113414786-A-G
• gnomAD v4: 11-113414786-A-G
• MyVariant Identifiers: chr11:g.113285508A>G (hg19) ; chr11:g.113414786A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414786A>G , CM000673.2:g.113414786A>G	GRCh38
NC_000011.9:g.113285508A>G , CM000673.1:g.113285508A>G	GRCh37
NC_000011.8:g.112790718A>G	NCBI36
NG_008841.1:g.65494T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.724-325T>C MANE Select	ENSP00000354859.3:n.724-325T>C
ENST00000346454.7:c.723+635T>C	ENSP00000278597.5:n.723+635T>C
ENST00000362072.7:c.724-325T>C	ENSP00000354859.3:n.724-325T>C
ENST00000535984.1:n.443-325T>C
ENST00000538967.5:c.724-325T>C	ENSP00000438215.1:n.724-325T>C
ENST00000540600.5:n.789-325T>C
ENST00000542968.5:c.724-325T>C	ENSP00000442172.1:n.724-325T>C
ENST00000544518.5:c.721-325T>C	ENSP00000441068.1:n.721-325T>C
NM_000795.3:c.724-325T>C	NP_000786.1:n.724-325T>C
NM_016574.3:c.723+635T>C	NP_057658.2:n.723+635T>C
XM_017017296.2:c.724-325T>C	XP_016872785.1:n.724-325T>C
NM_000795.4:c.724-325T>C MANE Select	NP_000786.1:n.724-325T>C
NM_016574.4:c.723+635T>C	NP_057658.2:n.723+635T>C