Canonical Allele Identifier: CA2843467029
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410709T>C , CM000673.2:g.113410709T>C GRCh38
NC_000011.9:g.113281431T>C , CM000673.1:g.113281431T>C GRCh37
NC_000011.8:g.112786641T>C NCBI36
NG_008841.1:g.69571A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*18A>G MANE Select ENSP00000354859.3:n.*18A>G
ENST00000346454.7:c.*18A>G ENSP00000278597.5:n.*18A>G
ENST00000362072.7:c.*18A>G ENSP00000354859.3:n.*18A>G
ENST00000538967.5:c.1356A>G ENSP00000438215.1:n.1356A>G
ENST00000542968.5:c.*18A>G ENSP00000442172.1:n.*18A>G
ENST00000544518.5:c.*18A>G ENSP00000441068.1:n.*18A>G
NM_000795.3:c.*18A>G NP_000786.1:n.*18A>G
NM_016574.3:c.*18A>G NP_057658.2:n.*18A>G
XM_017017296.2:c.*18A>G XP_016872785.1:n.*18A>G
NM_000795.4:c.*18A>G MANE Select NP_000786.1:n.*18A>G
NM_016574.4:c.*18A>G NP_057658.2:n.*18A>G