Canonical Allele Identifier: CA2616029351
Gene: DRD2 HGNC NCBI

Linked Data

gnomAD v4: 11-113410625-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410625G>T , CM000673.2:g.113410625G>T GRCh38
NC_000011.9:g.113281347G>T , CM000673.1:g.113281347G>T GRCh37
NC_000011.8:g.112786557G>T NCBI36
NG_008841.1:g.69655C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*102C>A MANE Select ENSP00000354859.3:n.*102C>A
ENST00000346454.7:c.*102C>A ENSP00000278597.5:n.*102C>A
ENST00000362072.7:c.*102C>A ENSP00000354859.3:n.*102C>A
ENST00000538967.5:c.1440C>A ENSP00000438215.1:n.1440C>A
ENST00000542968.5:c.*102C>A ENSP00000442172.1:n.*102C>A
ENST00000544518.5:c.*102C>A ENSP00000441068.1:n.*102C>A
NM_000795.3:c.*102C>A NP_000786.1:n.*102C>A
NM_016574.3:c.*102C>A NP_057658.2:n.*102C>A
XM_017017296.2:c.*102C>A XP_016872785.1:n.*102C>A
NM_000795.4:c.*102C>A MANE Select NP_000786.1:n.*102C>A
NM_016574.4:c.*102C>A NP_057658.2:n.*102C>A
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