Canonical Allele Identifier: CA472436484
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1389238182
gnomAD v2: 11-637586-C-T
gnomAD v4: 11-637586-C-T
MyVariant Identifiers: chr11:g.637586C>T (hg19) chr11:g.637586C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637586C>T , CM000673.2:g.637586C>T GRCh38
NC_000011.9:g.637586C>T , CM000673.1:g.637586C>T GRCh37
NC_000011.8:g.627586C>T NCBI36
NG_021241.1:g.5282C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.282C>T MANE Select ENSP00000176183.5:p.Ser94=
ENST00000176183.5:c.282C>T ENSP00000176183.5:p.Ser94=
NM_000797.3:c.282C>T NP_000788.2:p.Ser94=
NM_000797.4:c.282C>T MANE Select NP_000788.2:p.Ser94=
Search 100 bp 5'
Search 100 bp 3'