Canonical Allele Identifier: CA2616029194

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410490-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410490T>A , CM000673.2:g.113410490T>A	GRCh38
NC_000011.9:g.113281212T>A , CM000673.1:g.113281212T>A	GRCh37
NC_000011.8:g.112786422T>A	NCBI36
NG_008841.1:g.69790A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.*237A>T MANE Select	ENSP00000354859.3:n.*237A>T
ENST00000346454.7:c.*237A>T	ENSP00000278597.5:n.*237A>T
ENST00000362072.7:c.*237A>T	ENSP00000354859.3:n.*237A>T
ENST00000542968.5:c.*237A>T	ENSP00000442172.1:n.*237A>T
ENST00000544518.5:c.*237A>T	ENSP00000441068.1:n.*237A>T
NM_000795.3:c.*237A>T	NP_000786.1:n.*237A>T
NM_016574.3:c.*237A>T	NP_057658.2:n.*237A>T
XM_017017296.2:c.*237A>T	XP_016872785.1:n.*237A>T
NM_000795.4:c.*237A>T MANE Select	NP_000786.1:n.*237A>T
NM_016574.4:c.*237A>T	NP_057658.2:n.*237A>T