Canonical Allele Identifier: CA382650243

Gene: DRD2

Linked Data

• dbSNP Id: rs1199434420
• gnomAD v2: 11-113283473-G-T
• MyVariant Identifiers: chr11:g.113283473G>T (hg19) ; chr11:g.113412751G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412751G>T , CM000673.2:g.113412751G>T	GRCh38
NC_000011.9:g.113283473G>T , CM000673.1:g.113283473G>T	GRCh37
NC_000011.8:g.112788683G>T	NCBI36
NG_008841.1:g.67529C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.943C>A MANE Select	ENSP00000354859.3:p.Leu315Ile
ENST00000346454.7:c.856C>A	ENSP00000278597.5:p.Leu286Ile
ENST00000362072.7:c.943C>A	ENSP00000354859.3:p.Leu315Ile
ENST00000538967.5:c.949C>A	ENSP00000438215.1:p.Leu317Ile
ENST00000542968.5:c.943C>A	ENSP00000442172.1:p.Leu315Ile
ENST00000544518.5:c.940C>A	ENSP00000441068.1:p.Leu314Ile
NM_000795.3:c.943C>A	NP_000786.1:p.Leu315Ile
NM_016574.3:c.856C>A	NP_057658.2:p.Leu286Ile
XM_017017296.2:c.943C>A	XP_016872785.1:p.Leu315Ile
NM_000795.4:c.943C>A MANE Select	NP_000786.1:p.Leu315Ile
NM_016574.4:c.856C>A	NP_057658.2:p.Leu286Ile