Canonical Allele Identifier: CA2616029405

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410684-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410684C>G , CM000673.2:g.113410684C>G	GRCh38
NC_000011.9:g.113281406C>G , CM000673.1:g.113281406C>G	GRCh37
NC_000011.8:g.112786616C>G	NCBI36
NG_008841.1:g.69596G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*43G>C MANE Select	ENSP00000354859.3:n.*43G>C
ENST00000346454.7:c.*43G>C	ENSP00000278597.5:n.*43G>C
ENST00000362072.7:c.*43G>C	ENSP00000354859.3:n.*43G>C
ENST00000538967.5:c.1381G>C	ENSP00000438215.1:n.1381G>C
ENST00000542968.5:c.*43G>C	ENSP00000442172.1:n.*43G>C
ENST00000544518.5:c.*43G>C	ENSP00000441068.1:n.*43G>C
NM_000795.3:c.*43G>C	NP_000786.1:n.*43G>C
NM_016574.3:c.*43G>C	NP_057658.2:n.*43G>C
XM_017017296.2:c.*43G>C	XP_016872785.1:n.*43G>C
NM_000795.4:c.*43G>C MANE Select	NP_000786.1:n.*43G>C
NM_016574.4:c.*43G>C	NP_057658.2:n.*43G>C