Canonical Allele Identifier: CA476817059

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113281518C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410796C>G , CM000673.2:g.113410796C>G	GRCh38
NC_000011.9:g.113281518C>G , CM000673.1:g.113281518C>G	GRCh37
NC_000011.8:g.112786728C>G	NCBI36
NG_008841.1:g.69484G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1263G>C MANE Select	ENSP00000354859.3:p.Val421=
ENST00000346454.7:c.1176G>C	ENSP00000278597.5:p.Val392=
ENST00000362072.7:c.1263G>C	ENSP00000354859.3:p.Val421=
ENST00000538967.5:c.1269G>C	ENSP00000438215.1:p.Val423=
ENST00000542968.5:c.1263G>C	ENSP00000442172.1:p.Val421=
ENST00000544518.5:c.1260G>C	ENSP00000441068.1:p.Val420=
NM_000795.3:c.1263G>C	NP_000786.1:p.Val421=
NM_016574.3:c.1176G>C	NP_057658.2:p.Val392=
XM_017017296.2:c.1263G>C	XP_016872785.1:p.Val421=
NM_000795.4:c.1263G>C MANE Select	NP_000786.1:p.Val421=
NM_016574.4:c.1176G>C	NP_057658.2:p.Val392=