Canonical Allele Identifier: CA6281231

Gene: DRD2

Linked Data

• ClinVar Variation Id: 1079865
• ClinVar RCV Id: RCV001395284
• dbSNP Id: rs146497846
• ExAC: 11:113283492 G / A
• gnomAD v2: 11-113283492-G-A
• gnomAD v3: 11-113412770-G-A
• gnomAD v4: 11-113412770-G-A
• MyVariant Identifiers: chr11:g.113283492G>A (hg19) ; chr11:g.113412770G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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