Canonical Allele Identifier: CA379002505
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs780467485
gnomAD v4: 11-637426-G-A
MyVariant Identifiers: chr11:g.637426G>A (hg19) chr11:g.637426G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637426G>A , CM000673.2:g.637426G>A GRCh38
NC_000011.9:g.637426G>A , CM000673.1:g.637426G>A GRCh37
NC_000011.8:g.627426G>A NCBI36
NG_021241.1:g.5122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.122G>A MANE Select ENSP00000176183.5:p.Gly41Asp
ENST00000176183.5:c.122G>A ENSP00000176183.5:p.Gly41Asp
NM_000797.3:c.122G>A NP_000788.2:p.Gly41Asp
NM_000797.4:c.122G>A MANE Select NP_000788.2:p.Gly41Asp
Search 100 bp 5'
Search 100 bp 3'