Canonical Allele Identifier: CA379002867
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs755662323
gnomAD v4: 11-637569-C-G
MyVariant Identifiers: chr11:g.637569C>G (hg19) chr11:g.637569C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637569C>G , CM000673.2:g.637569C>G GRCh38
NC_000011.9:g.637569C>G , CM000673.1:g.637569C>G GRCh37
NC_000011.8:g.627569C>G NCBI36
NG_021241.1:g.5265C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.265C>G MANE Select ENSP00000176183.5:p.Pro89Ala
ENST00000176183.5:c.265C>G ENSP00000176183.5:p.Pro89Ala
NM_000797.3:c.265C>G NP_000788.2:p.Pro89Ala
NM_000797.4:c.265C>G MANE Select NP_000788.2:p.Pro89Ala
Search 100 bp 5'
Search 100 bp 3'