Canonical Allele Identifier: CA1947202080
Gene: DRD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640262C= , CM000673.2:g.640262C= GRCh38
NC_000011.9:g.640262C= , CM000673.1:g.640262C= GRCh37
NC_000011.8:g.630262C= NCBI36
NG_021241.1:g.7958C=

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1013C= MANE Select ENSP00000176183.5:p.Thr338=
ENST00000176183.5:c.1013C= ENSP00000176183.5:p.Thr338=
NM_000797.3:c.1013C= NP_000788.2:p.Thr338=
NM_000797.4:c.1013C= MANE Select NP_000788.2:p.Thr338=