Canonical Allele Identifier: CA472437122
Gene: DRD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.640248G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640248G>A , CM000673.2:g.640248G>A GRCh38
NC_000011.9:g.640248G>A , CM000673.1:g.640248G>A GRCh37
NC_000011.8:g.630248G>A NCBI36
NG_021241.1:g.7944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.999G>A MANE Select ENSP00000176183.5:p.Arg333=
ENST00000176183.5:c.999G>A ENSP00000176183.5:p.Arg333=
NM_000797.3:c.999G>A NP_000788.2:p.Arg333=
NM_000797.4:c.999G>A MANE Select NP_000788.2:p.Arg333=