Canonical Allele Identifier: CA6281228

Gene: DRD2

Linked Data

• dbSNP Id: rs373984882
• ExAC: 11:113283487 G / A
• gnomAD v2: 11-113283487-G-A
• gnomAD v3: 11-113412765-G-A
• gnomAD v4: 11-113412765-G-A
• MyVariant Identifiers: chr11:g.113283487G>A (hg19) ; chr11:g.113412765G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412765G>A , CM000673.2:g.113412765G>A	GRCh38
NC_000011.9:g.113283487G>A , CM000673.1:g.113283487G>A	GRCh37
NC_000011.8:g.112788697G>A	NCBI36
NG_008841.1:g.67515C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.929C>T MANE Select	ENSP00000354859.3:p.Pro310Leu
ENST00000346454.7:c.842C>T	ENSP00000278597.5:p.Pro281Leu
ENST00000362072.7:c.929C>T	ENSP00000354859.3:p.Pro310Leu
ENST00000538967.5:c.935C>T	ENSP00000438215.1:p.Pro312Leu
ENST00000542968.5:c.929C>T	ENSP00000442172.1:p.Pro310Leu
ENST00000544518.5:c.926C>T	ENSP00000441068.1:p.Pro309Leu
NM_000795.3:c.929C>T	NP_000786.1:p.Pro310Leu
NM_016574.3:c.842C>T	NP_057658.2:p.Pro281Leu
XM_017017296.2:c.929C>T	XP_016872785.1:p.Pro310Leu
NM_000795.4:c.929C>T MANE Select	NP_000786.1:p.Pro310Leu
NM_016574.4:c.842C>T	NP_057658.2:p.Pro281Leu