Canonical Allele Identifier: CA228635608

Gene: DRD2

Linked Data

• dbSNP Id: rs776101879
• gnomAD v3: 11-113439569-G-T
• gnomAD v4: 11-113439569-G-T
• MyVariant Identifiers: chr11:g.113310291G>T (hg19) ; chr11:g.113439569G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439569G>T , CM000673.2:g.113439569G>T	GRCh38
NC_000011.9:g.113310291G>T , CM000673.1:g.113310291G>T	GRCh37
NC_000011.8:g.112815501G>T	NCBI36
NG_008841.1:g.40711C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-14887C>A MANE Select	ENSP00000354859.3:n.-31-14887C>A
ENST00000346454.7:c.-31-14887C>A	ENSP00000278597.5:n.-31-14887C>A
ENST00000362072.7:c.-31-14887C>A	ENSP00000354859.3:n.-31-14887C>A
ENST00000540600.5:n.35-14887C>A
ENST00000542616.1:c.-31-14887C>A	ENSP00000441474.1:n.-31-14887C>A
ENST00000543292.1:c.-32+8002C>A	ENSP00000438419.1:n.-32+8002C>A
NM_000795.3:c.-31-14887C>A	NP_000786.1:n.-31-14887C>A
NM_016574.3:c.-31-14887C>A	NP_057658.2:n.-31-14887C>A
XM_017017296.2:c.-31-14887C>A	XP_016872785.1:n.-31-14887C>A
NM_000795.4:c.-31-14887C>A MANE Select	NP_000786.1:n.-31-14887C>A
NM_016574.4:c.-31-14887C>A	NP_057658.2:n.-31-14887C>A