Canonical Allele Identifier: CA379002873
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs530031052
gnomAD v3: 11-637570-C-A
gnomAD v4: 11-637570-C-A
MyVariant Identifiers: chr11:g.637570C>A (hg19) chr11:g.637570C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637570C>A , CM000673.2:g.637570C>A GRCh38
NC_000011.9:g.637570C>A , CM000673.1:g.637570C>A GRCh37
NC_000011.8:g.627570C>A NCBI36
NG_021241.1:g.5266C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.266C>A MANE Select ENSP00000176183.5:p.Pro89Gln
ENST00000176183.5:c.266C>A ENSP00000176183.5:p.Pro89Gln
NM_000797.3:c.266C>A NP_000788.2:p.Pro89Gln
NM_000797.4:c.266C>A MANE Select NP_000788.2:p.Pro89Gln
Search 100 bp 5'
Search 100 bp 3'