Canonical Allele Identifier: CA379008443
Gene: DRD4 HGNC NCBI

Linked Data

gnomAD v4: 11-640261-A-G
MyVariant Identifiers: chr11:g.640261A>G (hg19) chr11:g.640261A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640261A>G , CM000673.2:g.640261A>G GRCh38
NC_000011.9:g.640261A>G , CM000673.1:g.640261A>G GRCh37
NC_000011.8:g.630261A>G NCBI36
NG_021241.1:g.7957A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000176183.6:c.1012A>G MANE Select ENSP00000176183.5:p.Thr338Ala
ENST00000176183.5:c.1012A>G ENSP00000176183.5:p.Thr338Ala
NM_000797.3:c.1012A>G NP_000788.2:p.Thr338Ala
NM_000797.4:c.1012A>G MANE Select NP_000788.2:p.Thr338Ala
Search 100 bp 5'
Search 100 bp 3'