Canonical Allele Identifier: CA6281230
Gene: DRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2729438
ClinVar RCV Id: RCV003587268
dbSNP Id: rs149926361
ExAC: 11:113283491 C / T
gnomAD v2: 11-113283491-C-T
gnomAD v3: 11-113412769-C-T
gnomAD v4: 11-113412769-C-T
MyVariant Identifiers: chr11:g.113283491C>T (hg19) chr11:g.113412769C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412769C>T , CM000673.2:g.113412769C>T GRCh38
NC_000011.9:g.113283491C>T , CM000673.1:g.113283491C>T GRCh37
NC_000011.8:g.112788701C>T NCBI36
NG_008841.1:g.67511G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.925G>A MANE Select ENSP00000354859.3:p.Asp309Asn
ENST00000346454.7:c.838G>A ENSP00000278597.5:p.Asp280Asn
ENST00000362072.7:c.925G>A ENSP00000354859.3:p.Asp309Asn
ENST00000538967.5:c.931G>A ENSP00000438215.1:p.Asp311Asn
ENST00000542968.5:c.925G>A ENSP00000442172.1:p.Asp309Asn
ENST00000544518.5:c.922G>A ENSP00000441068.1:p.Asp308Asn
NM_000795.3:c.925G>A NP_000786.1:p.Asp309Asn
NM_016574.3:c.838G>A NP_057658.2:p.Asp280Asn
XM_017017296.2:c.925G>A XP_016872785.1:p.Asp309Asn
NM_000795.4:c.925G>A MANE Select NP_000786.1:p.Asp309Asn
NM_016574.4:c.838G>A NP_057658.2:p.Asp280Asn
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