Canonical Allele Identifier: CA5785908
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs773478489
gnomAD v4: 11-640339-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640339G>A , CM000673.2:g.640339G>A GRCh38
NC_000011.9:g.640339G>A , CM000673.1:g.640339G>A GRCh37
NC_000011.8:g.630339G>A NCBI36
NG_021241.1:g.8035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+33G>A MANE Select ENSP00000176183.5:n.1057+33G>A
ENST00000176183.5:c.1057+33G>A ENSP00000176183.5:n.1057+33G>A
NM_000797.3:c.1057+33G>A NP_000788.2:n.1057+33G>A
NM_000797.4:c.1057+33G>A MANE Select NP_000788.2:n.1057+33G>A