Canonical Allele Identifier: CA477043096
Gene: DRD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113283399C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412677C>T , CM000673.2:g.113412677C>T GRCh38
NC_000011.9:g.113283399C>T , CM000673.1:g.113283399C>T GRCh37
NC_000011.8:g.112788609C>T NCBI36
NG_008841.1:g.67603G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1017G>A MANE Select ENSP00000354859.3:p.Lys339=
ENST00000346454.7:c.930G>A ENSP00000278597.5:p.Lys310=
ENST00000362072.7:c.1017G>A ENSP00000354859.3:p.Lys339=
ENST00000538967.5:c.1023G>A ENSP00000438215.1:p.Lys341=
ENST00000542968.5:c.1017G>A ENSP00000442172.1:p.Lys339=
ENST00000544518.5:c.1014G>A ENSP00000441068.1:p.Lys338=
NM_000795.3:c.1017G>A NP_000786.1:p.Lys339=
NM_016574.3:c.930G>A NP_057658.2:p.Lys310=
XM_017017296.2:c.1017G>A XP_016872785.1:p.Lys339=
NM_000795.4:c.1017G>A MANE Select NP_000786.1:p.Lys339=
NM_016574.4:c.930G>A NP_057658.2:p.Lys310=