Canonical Allele Identifier: CA597020844
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs989509727
gnomAD v2: 11-640343-G-GC
gnomAD v4: 11-640343-G-GC
MyVariant Identifiers: chr11:g.640343_640344insC (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640343_640344insC , CM000673.2:g.640343_640344insC GRCh38
NC_000011.9:g.640343_640344insC , CM000673.1:g.640343_640344insC GRCh37
NC_000011.8:g.630343_630344insC NCBI36
NG_021241.1:g.8039_8040insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+37_1057+38insC MANE Select ENSP00000176183.5:n.1057+37_1057+38insC
ENST00000176183.5:c.1057+37_1057+38insC ENSP00000176183.5:n.1057+37_1057+38insC
NM_000797.3:c.1057+37_1057+38insC NP_000788.2:n.1057+37_1057+38insC
NM_000797.4:c.1057+37_1057+38insC MANE Select NP_000788.2:n.1057+37_1057+38insC
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