Canonical Allele Identifier: CA382649930

Gene: DRD2

Linked Data

• gnomAD v4: 11-113412676-T-C
• MyVariant Identifiers: chr11:g.113283398T>C (hg19) ; chr11:g.113412676T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412676T>C , CM000673.2:g.113412676T>C	GRCh38
NC_000011.9:g.113283398T>C , CM000673.1:g.113283398T>C	GRCh37
NC_000011.8:g.112788608T>C	NCBI36
NG_008841.1:g.67604A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1018A>G MANE Select	ENSP00000354859.3:p.Ile340Val
ENST00000346454.7:c.931A>G	ENSP00000278597.5:p.Ile311Val
ENST00000362072.7:c.1018A>G	ENSP00000354859.3:p.Ile340Val
ENST00000538967.5:c.1024A>G	ENSP00000438215.1:p.Ile342Val
ENST00000542968.5:c.1018A>G	ENSP00000442172.1:p.Ile340Val
ENST00000544518.5:c.1015A>G	ENSP00000441068.1:p.Ile339Val
NM_000795.3:c.1018A>G	NP_000786.1:p.Ile340Val
NM_016574.3:c.931A>G	NP_057658.2:p.Ile311Val
XM_017017296.2:c.1018A>G	XP_016872785.1:p.Ile340Val
NM_000795.4:c.1018A>G MANE Select	NP_000786.1:p.Ile340Val
NM_016574.4:c.931A>G	NP_057658.2:p.Ile311Val