Canonical Allele Identifier: CA942371599
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1951067226
gnomAD v3: 11-113439555-CA-C
gnomAD v4: 11-113439555-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439556del , CM000673.2:g.113439556del GRCh38
NC_000011.9:g.113310278del , CM000673.1:g.113310278del GRCh37
NC_000011.8:g.112815488del NCBI36
NG_008841.1:g.40724del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14874del MANE Select ENSP00000354859.3:n.-31-14874del
ENST00000346454.7:c.-31-14874del ENSP00000278597.5:n.-31-14874del
ENST00000362072.7:c.-31-14874del ENSP00000354859.3:n.-31-14874del
ENST00000540600.5:n.35-14874del
ENST00000542616.1:c.-31-14874del ENSP00000441474.1:n.-31-14874del
ENST00000543292.1:c.-32+8015del ENSP00000438419.1:n.-32+8015del
NM_000795.3:c.-31-14874del NP_000786.1:n.-31-14874del
NM_016574.3:c.-31-14874del NP_057658.2:n.-31-14874del
XM_017017296.2:c.-31-14874del XP_016872785.1:n.-31-14874del
NM_000795.4:c.-31-14874del MANE Select NP_000786.1:n.-31-14874del
NM_016574.4:c.-31-14874del NP_057658.2:n.-31-14874del
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