Canonical Allele Identifier: CA597020839
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs773478489
gnomAD v2: 11-640339-G-C
gnomAD v3: 11-640339-G-C
gnomAD v4: 11-640339-G-C
MyVariant Identifiers: chr11:g.640339G>C (hg19) chr11:g.640339_640341delinsCGA (hg19) chr11:g.640339G>C (hg38) chr11:g.640339_640341delinsCGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.640339G>C , CM000673.2:g.640339G>C GRCh38
NC_000011.9:g.640339G>C , CM000673.1:g.640339G>C GRCh37
NC_000011.8:g.630339G>C NCBI36
NG_021241.1:g.8035G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.1057+33G>C MANE Select ENSP00000176183.5:n.1057+33G>C
ENST00000176183.5:c.1057+33G>C ENSP00000176183.5:n.1057+33G>C
NM_000797.3:c.1057+33G>C NP_000788.2:n.1057+33G>C
NM_000797.4:c.1057+33G>C MANE Select NP_000788.2:n.1057+33G>C
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