Canonical Allele Identifier: CA597020859
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1419534568
gnomAD v2: 11-637625-G-A
gnomAD v4: 11-637625-G-A
MyVariant Identifiers: chr11:g.637625G>A (hg19) chr11:g.637625G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637625G>A , CM000673.2:g.637625G>A GRCh38
NC_000011.9:g.637625G>A , CM000673.1:g.637625G>A GRCh37
NC_000011.8:g.627625G>A NCBI36
NG_021241.1:g.5321G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.285+36G>A MANE Select ENSP00000176183.5:n.285+36G>A
ENST00000176183.5:c.285+36G>A ENSP00000176183.5:n.285+36G>A
NM_000797.3:c.285+36G>A NP_000788.2:n.285+36G>A
NM_000797.4:c.285+36G>A MANE Select NP_000788.2:n.285+36G>A
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