Canonical Allele Identifier: CA2001188668
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1951474028
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475362C>A , CM000673.2:g.113475362C>A GRCh38
NC_000011.9:g.113346084C>A , CM000673.1:g.113346084C>A GRCh37
NC_000011.8:g.112851294C>A NCBI36
NG_008841.1:g.4918G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-318G>T MANE Select ENSP00000354859.3:n.-318G>T
ENST00000362072.7:c.-318G>T ENSP00000354859.3:n.-318G>T
ENST00000540600.5:n.34+296G>T
NM_000795.4:c.-318G>T MANE Select NP_000786.1:n.-318G>T
NM_016574.4:c.-318G>T NP_057658.2:n.-318G>T
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