Canonical Allele Identifier: CA2838590429
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410708G>T , CM000673.2:g.113410708G>T GRCh38
NC_000011.9:g.113281430G>T , CM000673.1:g.113281430G>T GRCh37
NC_000011.8:g.112786640G>T NCBI36
NG_008841.1:g.69572C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*19C>A MANE Select ENSP00000354859.3:n.*19C>A
ENST00000346454.7:c.*19C>A ENSP00000278597.5:n.*19C>A
ENST00000362072.7:c.*19C>A ENSP00000354859.3:n.*19C>A
ENST00000538967.5:c.1357C>A ENSP00000438215.1:n.1357C>A
ENST00000542968.5:c.*19C>A ENSP00000442172.1:n.*19C>A
ENST00000544518.5:c.*19C>A ENSP00000441068.1:n.*19C>A
NM_000795.3:c.*19C>A NP_000786.1:n.*19C>A
NM_016574.3:c.*19C>A NP_057658.2:n.*19C>A
XM_017017296.2:c.*19C>A XP_016872785.1:n.*19C>A
NM_000795.4:c.*19C>A MANE Select NP_000786.1:n.*19C>A
NM_016574.4:c.*19C>A NP_057658.2:n.*19C>A