Canonical Allele Identifier: CA382649074

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410797-A-C
• MyVariant Identifiers: chr11:g.113281519A>C (hg19) ; chr11:g.113410797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410797A>C , CM000673.2:g.113410797A>C	GRCh38
NC_000011.9:g.113281519A>C , CM000673.1:g.113281519A>C	GRCh37
NC_000011.8:g.112786729A>C	NCBI36
NG_008841.1:g.69483T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1262T>G MANE Select	ENSP00000354859.3:p.Val421Gly
ENST00000346454.7:c.1175T>G	ENSP00000278597.5:p.Val392Gly
ENST00000362072.7:c.1262T>G	ENSP00000354859.3:p.Val421Gly
ENST00000538967.5:c.1268T>G	ENSP00000438215.1:p.Val423Gly
ENST00000542968.5:c.1262T>G	ENSP00000442172.1:p.Val421Gly
ENST00000544518.5:c.1259T>G	ENSP00000441068.1:p.Val420Gly
NM_000795.3:c.1262T>G	NP_000786.1:p.Val421Gly
NM_016574.3:c.1175T>G	NP_057658.2:p.Val392Gly
XM_017017296.2:c.1262T>G	XP_016872785.1:p.Val421Gly
NM_000795.4:c.1262T>G MANE Select	NP_000786.1:p.Val421Gly
NM_016574.4:c.1175T>G	NP_057658.2:p.Val392Gly