Canonical Allele Identifier: CA5785567
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs768493668
gnomAD v2: 11-637541-C-A
gnomAD v3: 11-637541-C-A
gnomAD v4: 11-637541-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637541C>A , CM000673.2:g.637541C>A GRCh38
NC_000011.9:g.637541C>A , CM000673.1:g.637541C>A GRCh37
NC_000011.8:g.627541C>A NCBI36
NG_021241.1:g.5237C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.237C>A MANE Select ENSP00000176183.5:p.Ala79=
ENST00000176183.5:c.237C>A ENSP00000176183.5:p.Ala79=
NM_000797.3:c.237C>A NP_000788.2:p.Ala79=
NM_000797.4:c.237C>A MANE Select NP_000788.2:p.Ala79=