Canonical Allele Identifier: CA216942825
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs12720387
gnomAD v4: 11-637621-A-C
MyVariant Identifiers: chr11:g.637621A>C (hg19) chr11:g.637621A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637621A>C , CM000673.2:g.637621A>C GRCh38
NC_000011.9:g.637621A>C , CM000673.1:g.637621A>C GRCh37
NC_000011.8:g.627621A>C NCBI36
NG_021241.1:g.5317A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.285+32A>C MANE Select ENSP00000176183.5:n.285+32A>C
ENST00000176183.5:c.285+32A>C ENSP00000176183.5:n.285+32A>C
NM_000797.3:c.285+32A>C NP_000788.2:n.285+32A>C
NM_000797.4:c.285+32A>C MANE Select NP_000788.2:n.285+32A>C
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