Canonical Allele Identifier: CA5785515
Gene: DRD4 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.637294C>T
GRCh37 chr11:g.637294C>T
gnomAD v2:
11:637294 C / T
gnomAD v3:
11:637294 C / T
gnomAD v4:
chr11-637294-C-T
Joint Max Group AF 0.07596462 (SAS)
Genomes Max Group AF 0.06586325 (SAS)
Exomes Max Group AF 0.0770663 (SAS)
ClinVar RCV:
RCV003239302
ClinVar Variation:
2507404
dbSNP:
146680769
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637294C>T , CM000673.2:g.637294C>T GRCh38
NC_000011.9:g.637294C>T , CM000673.1:g.637294C>T GRCh37
NC_000011.8:g.627294C>T NCBI36
NG_021241.1:g.4990C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.-11C>T MANE Select ENSP00000176183.5:n.-11C>T
ENST00000176183.5:c.-11C>T ENSP00000176183.5:n.-11C>T
NM_000797.4:c.-11C>T MANE Select NP_000788.2:n.-11C>T
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