Canonical Allele Identifier: CA472437195
Gene: DRD4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.640206C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640206C>A , CM000673.2:g.640206C>A GRCh38
NC_000011.9:g.640206C>A , CM000673.1:g.640206C>A GRCh37
NC_000011.8:g.630206C>A NCBI36
NG_021241.1:g.7902C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.957C>A MANE Select ENSP00000176183.5:p.Ala319=
ENST00000176183.5:c.957C>A ENSP00000176183.5:p.Ala319=
NM_000797.3:c.957C>A NP_000788.2:p.Ala319=
NM_000797.4:c.957C>A MANE Select NP_000788.2:p.Ala319=