Canonical Allele Identifier: CA472436460
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1564911937
gnomAD v4: 11-637574-C-G
MyVariant Identifiers: chr11:g.637574C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637574C>G , CM000673.2:g.637574C>G GRCh38
NC_000011.9:g.637574C>G , CM000673.1:g.637574C>G GRCh37
NC_000011.8:g.627574C>G NCBI36
NG_021241.1:g.5270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.270C>G MANE Select ENSP00000176183.5:p.Leu90=
ENST00000176183.5:c.270C>G ENSP00000176183.5:p.Leu90=
NM_000797.3:c.270C>G NP_000788.2:p.Leu90=
NM_000797.4:c.270C>G MANE Select NP_000788.2:p.Leu90=
Search 100 bp 5'
Search 100 bp 3'