Canonical Allele Identifier: CA382650250

Gene: DRD2

Linked Data

• dbSNP Id: rs770907631
• gnomAD v2: 11-113283476-C-A
• gnomAD v4: 11-113412754-C-A
• MyVariant Identifiers: chr11:g.113283476C>A (hg19) ; chr11:g.113412754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412754C>A , CM000673.2:g.113412754C>A	GRCh38
NC_000011.9:g.113283476C>A , CM000673.1:g.113283476C>A	GRCh37
NC_000011.8:g.112788686C>A	NCBI36
NG_008841.1:g.67526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.940G>T MANE Select	ENSP00000354859.3:p.Gly314Cys
ENST00000346454.7:c.853G>T	ENSP00000278597.5:p.Gly285Cys
ENST00000362072.7:c.940G>T	ENSP00000354859.3:p.Gly314Cys
ENST00000538967.5:c.946G>T	ENSP00000438215.1:p.Gly316Cys
ENST00000542968.5:c.940G>T	ENSP00000442172.1:p.Gly314Cys
ENST00000544518.5:c.937G>T	ENSP00000441068.1:p.Gly313Cys
NM_000795.3:c.940G>T	NP_000786.1:p.Gly314Cys
NM_016574.3:c.853G>T	NP_057658.2:p.Gly285Cys
XM_017017296.2:c.940G>T	XP_016872785.1:p.Gly314Cys
NM_000795.4:c.940G>T MANE Select	NP_000786.1:p.Gly314Cys
NM_016574.4:c.853G>T	NP_057658.2:p.Gly285Cys