Canonical Allele Identifier: CA6281208
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs752896247

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412692G>C , CM000673.2:g.113412692G>C GRCh38
NC_000011.9:g.113283414G>C , CM000673.1:g.113283414G>C GRCh37
NC_000011.8:g.112788624G>C NCBI36
NG_008841.1:g.67588C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1002C>G MANE Select ENSP00000354859.3:p.His334Gln
ENST00000346454.7:c.915C>G ENSP00000278597.5:p.His305Gln
ENST00000362072.7:c.1002C>G ENSP00000354859.3:p.His334Gln
ENST00000538967.5:c.1008C>G ENSP00000438215.1:p.His336Gln
ENST00000542968.5:c.1002C>G ENSP00000442172.1:p.His334Gln
ENST00000544518.5:c.999C>G ENSP00000441068.1:p.His333Gln
NM_000795.3:c.1002C>G NP_000786.1:p.His334Gln
NM_016574.3:c.915C>G NP_057658.2:p.His305Gln
XM_017017296.2:c.1002C>G XP_016872785.1:p.His334Gln
NM_000795.4:c.1002C>G MANE Select NP_000786.1:p.His334Gln
NM_016574.4:c.915C>G NP_057658.2:p.His305Gln