Canonical Allele Identifier: CA382649075

Gene: DRD2

Linked Data

• dbSNP Id: rs1950761768
• gnomAD v3: 11-113410797-A-G
• gnomAD v4: 11-113410797-A-G
• MyVariant Identifiers: chr11:g.113281519A>G (hg19) ; chr11:g.113410797A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1262T>C MANE Select	ENSP00000354859.3:p.Val421Ala
ENST00000346454.7:c.1175T>C	ENSP00000278597.5:p.Val392Ala
ENST00000362072.7:c.1262T>C	ENSP00000354859.3:p.Val421Ala
ENST00000538967.5:c.1268T>C	ENSP00000438215.1:p.Val423Ala
ENST00000542968.5:c.1262T>C	ENSP00000442172.1:p.Val421Ala
ENST00000544518.5:c.1259T>C	ENSP00000441068.1:p.Val420Ala
NM_000795.3:c.1262T>C	NP_000786.1:p.Val421Ala
NM_016574.3:c.1175T>C	NP_057658.2:p.Val392Ala
XM_017017296.2:c.1262T>C	XP_016872785.1:p.Val421Ala
NM_000795.4:c.1262T>C MANE Select	NP_000786.1:p.Val421Ala
NM_016574.4:c.1175T>C	NP_057658.2:p.Val392Ala