Canonical Allele Identifier: CA379008446
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1858198497
gnomAD v4: 11-640262-C-A
MyVariant Identifiers: chr11:g.640262C>A (hg19) chr11:g.640262C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1013C>A MANE Select ENSP00000176183.5:p.Thr338Asn
ENST00000176183.5:c.1013C>A ENSP00000176183.5:p.Thr338Asn
NM_000797.3:c.1013C>A NP_000788.2:p.Thr338Asn
NM_000797.4:c.1013C>A MANE Select NP_000788.2:p.Thr338Asn
Search 100 bp 5'
Search 100 bp 3'