Canonical Allele Identifier: CA382650277

Gene: DRD2

Linked Data

• dbSNP Id: rs1950781813
• gnomAD v4: 11-113412760-G-A
• MyVariant Identifiers: chr11:g.113283482G>A (hg19) ; chr11:g.113412760G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412760G>A , CM000673.2:g.113412760G>A	GRCh38
NC_000011.9:g.113283482G>A , CM000673.1:g.113283482G>A	GRCh37
NC_000011.8:g.112788692G>A	NCBI36
NG_008841.1:g.67520C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.934C>T MANE Select	ENSP00000354859.3:p.His312Tyr
ENST00000346454.7:c.847C>T	ENSP00000278597.5:p.His283Tyr
ENST00000362072.7:c.934C>T	ENSP00000354859.3:p.His312Tyr
ENST00000538967.5:c.940C>T	ENSP00000438215.1:p.His314Tyr
ENST00000542968.5:c.934C>T	ENSP00000442172.1:p.His312Tyr
ENST00000544518.5:c.931C>T	ENSP00000441068.1:p.His311Tyr
NM_000795.3:c.934C>T	NP_000786.1:p.His312Tyr
NM_016574.3:c.847C>T	NP_057658.2:p.His283Tyr
XM_017017296.2:c.934C>T	XP_016872785.1:p.His312Tyr
NM_000795.4:c.934C>T MANE Select	NP_000786.1:p.His312Tyr
NM_016574.4:c.847C>T	NP_057658.2:p.His283Tyr