Canonical Allele Identifier: CA597020850
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1443500723
gnomAD v2: 11-637593-A-G
gnomAD v4: 11-637593-A-G
MyVariant Identifiers: chr11:g.637593A>G (hg19) chr11:g.637593A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637593A>G , CM000673.2:g.637593A>G GRCh38
NC_000011.9:g.637593A>G , CM000673.1:g.637593A>G GRCh37
NC_000011.8:g.627593A>G NCBI36
NG_021241.1:g.5289A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.285+4A>G MANE Select ENSP00000176183.5:n.285+4A>G
ENST00000176183.5:c.285+4A>G ENSP00000176183.5:n.285+4A>G
NM_000797.3:c.285+4A>G NP_000788.2:n.285+4A>G
NM_000797.4:c.285+4A>G MANE Select NP_000788.2:n.285+4A>G
Search 100 bp 5'
Search 100 bp 3'