Canonical Allele Identifier: CA2001168987
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1950809123
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414824_113414826del , CM000673.2:g.113414824_113414826del GRCh38
NC_000011.9:g.113285546_113285548del , CM000673.1:g.113285546_113285548del GRCh37
NC_000011.8:g.112790756_112790758del NCBI36
NG_008841.1:g.65454_65456del

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.724-365_724-363del MANE Select ENSP00000354859.3:n.724-365_724-363del
ENST00000346454.7:c.723+595_723+597del ENSP00000278597.5:n.723+595_723+597del
ENST00000362072.7:c.724-365_724-363del ENSP00000354859.3:n.724-365_724-363del
ENST00000535984.1:n.443-365_443-363del
ENST00000538967.5:c.724-365_724-363del ENSP00000438215.1:n.724-365_724-363del
ENST00000540600.5:n.789-365_789-363del
ENST00000542968.5:c.724-365_724-363del ENSP00000442172.1:n.724-365_724-363del
ENST00000544518.5:c.721-365_721-363del ENSP00000441068.1:n.721-365_721-363del
NM_000795.3:c.724-365_724-363del NP_000786.1:n.724-365_724-363del
NM_016574.3:c.723+595_723+597del NP_057658.2:n.723+595_723+597del
XM_017017296.2:c.724-365_724-363del XP_016872785.1:n.724-365_724-363del
NM_000795.4:c.724-365_724-363del MANE Select NP_000786.1:n.724-365_724-363del
NM_016574.4:c.723+595_723+597del NP_057658.2:n.723+595_723+597del
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