Canonical Allele Identifier: CA216943584
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs34773603
MyVariant Identifiers: chr11:g.640450G>A (hg19) chr11:g.640450G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640450G>A , CM000673.2:g.640450G>A GRCh38
NC_000011.9:g.640450G>A , CM000673.1:g.640450G>A GRCh37
NC_000011.8:g.630450G>A NCBI36
NG_021241.1:g.8146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1107G>A MANE Select ENSP00000176183.5:p.Gln369=
ENST00000176183.5:c.1107G>A ENSP00000176183.5:p.Gln369=
NM_000797.3:c.1107G>A NP_000788.2:p.Gln369=
NM_000797.4:c.1107G>A MANE Select NP_000788.2:p.Gln369=
Search 100 bp 5'
Search 100 bp 3'