Canonical Allele Identifier: CA6281140

Gene: DRD2

Linked Data

• dbSNP Id: rs201801648
• ExAC: 11:113281457 G / A
• gnomAD v2: 11-113281457-G-A
• gnomAD v3: 11-113410735-G-A
• gnomAD v4: 11-113410735-G-A
• MyVariant Identifiers: chr11:g.113281457G>A (hg19) ; chr11:g.113410735G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410735G>A , CM000673.2:g.113410735G>A	GRCh38
NC_000011.9:g.113281457G>A , CM000673.1:g.113281457G>A	GRCh37
NC_000011.8:g.112786667G>A	NCBI36
NG_008841.1:g.69545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1324C>T MANE Select	ENSP00000354859.3:p.His442Tyr
ENST00000346454.7:c.1237C>T	ENSP00000278597.5:p.His413Tyr
ENST00000362072.7:c.1324C>T	ENSP00000354859.3:p.His442Tyr
ENST00000538967.5:c.1330C>T	ENSP00000438215.1:p.His444Tyr
ENST00000542968.5:c.1324C>T	ENSP00000442172.1:p.His442Tyr
ENST00000544518.5:c.1321C>T	ENSP00000441068.1:p.His441Tyr
NM_000795.3:c.1324C>T	NP_000786.1:p.His442Tyr
NM_016574.3:c.1237C>T	NP_057658.2:p.His413Tyr
XM_017017296.2:c.1324C>T	XP_016872785.1:p.His442Tyr
NM_000795.4:c.1324C>T MANE Select	NP_000786.1:p.His442Tyr
NM_016574.4:c.1237C>T	NP_057658.2:p.His413Tyr