Canonical Allele Identifier: CA6281141

Gene: DRD2

Linked Data

• ClinVar Variation Id: 416373
• ClinVar RCV Id: RCV000465239
• dbSNP Id: rs77930100
• ExAC: 11:113281476 C / T
• gnomAD v2: 11-113281476-C-T
• gnomAD v3: 11-113410754-C-T
• gnomAD v4: 11-113410754-C-T
• COSMIC: COSM3443523 ; COSM3443524
• MyVariant Identifiers: chr11:g.113281476C>T (hg19) ; chr11:g.113410754C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410754C>T , CM000673.2:g.113410754C>T	GRCh38
NC_000011.9:g.113281476C>T , CM000673.1:g.113281476C>T	GRCh37
NC_000011.8:g.112786686C>T	NCBI36
NG_008841.1:g.69526G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1305G>A MANE Select	ENSP00000354859.3:p.Lys435=
ENST00000346454.7:c.1218G>A	ENSP00000278597.5:p.Lys406=
ENST00000362072.7:c.1305G>A	ENSP00000354859.3:p.Lys435=
ENST00000538967.5:c.1311G>A	ENSP00000438215.1:p.Lys437=
ENST00000542968.5:c.1305G>A	ENSP00000442172.1:p.Lys435=
ENST00000544518.5:c.1302G>A	ENSP00000441068.1:p.Lys434=
NM_000795.3:c.1305G>A	NP_000786.1:p.Lys435=
NM_016574.3:c.1218G>A	NP_057658.2:p.Lys406=
XM_017017296.2:c.1305G>A	XP_016872785.1:p.Lys435=
NM_000795.4:c.1305G>A MANE Select	NP_000786.1:p.Lys435=
NM_016574.4:c.1218G>A	NP_057658.2:p.Lys406=