Canonical Allele Identifier: CA671867343
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs929372502
gnomAD v3: 11-113414836-CA-C
gnomAD v4: 11-113414836-CA-C
MyVariant Identifiers: chr11:g.113285559del (hg19) chr11:g.113414837del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414843del , CM000673.2:g.113414843del GRCh38
NC_000011.9:g.113285565del , CM000673.1:g.113285565del GRCh37
NC_000011.8:g.112790775del NCBI36
NG_008841.1:g.65443del

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.724-376del MANE Select ENSP00000354859.3:n.724-376del
ENST00000346454.7:c.723+584del ENSP00000278597.5:n.723+584del
ENST00000362072.7:c.724-376del ENSP00000354859.3:n.724-376del
ENST00000535984.1:n.443-376del
ENST00000538967.5:c.724-376del ENSP00000438215.1:n.724-376del
ENST00000540600.5:n.789-376del
ENST00000542968.5:c.724-376del ENSP00000442172.1:n.724-376del
ENST00000544518.5:c.721-376del ENSP00000441068.1:n.721-376del
NM_000795.3:c.724-376del NP_000786.1:n.724-376del
NM_016574.3:c.723+584del NP_057658.2:n.723+584del
XM_017017296.2:c.724-376del XP_016872785.1:n.724-376del
NM_000795.4:c.724-376del MANE Select NP_000786.1:n.724-376del
NM_016574.4:c.723+584del NP_057658.2:n.723+584del
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