Canonical Allele Identifier: CA2616029308

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410579-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410579C>T , CM000673.2:g.113410579C>T	GRCh38
NC_000011.9:g.113281301C>T , CM000673.1:g.113281301C>T	GRCh37
NC_000011.8:g.112786511C>T	NCBI36
NG_008841.1:g.69701G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*148G>A MANE Select	ENSP00000354859.3:n.*148G>A
ENST00000346454.7:c.*148G>A	ENSP00000278597.5:n.*148G>A
ENST00000362072.7:c.*148G>A	ENSP00000354859.3:n.*148G>A
ENST00000538967.5:c.1486G>A	ENSP00000438215.1:n.1486G>A
ENST00000542968.5:c.*148G>A	ENSP00000442172.1:n.*148G>A
ENST00000544518.5:c.*148G>A	ENSP00000441068.1:n.*148G>A
NM_000795.3:c.*148G>A	NP_000786.1:n.*148G>A
NM_016574.3:c.*148G>A	NP_057658.2:n.*148G>A
XM_017017296.2:c.*148G>A	XP_016872785.1:n.*148G>A
NM_000795.4:c.*148G>A MANE Select	NP_000786.1:n.*148G>A
NM_016574.4:c.*148G>A	NP_057658.2:n.*148G>A