Linked Data
ClinVar Variation Id:
437
dbSNP Id:
rs1801267
ExAC:
1:97564154 C / T
gnomAD v2:
1-97564154-C-T
gnomAD v3:
1-97098598-C-T
gnomAD v4:
1-97098598-C-T
PubMed:
PMID:9439663
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97098598C>T , CM000663.2:g.97098598C>T | GRCh38 |
| NC_000001.10:g.97564154C>T , CM000663.1:g.97564154C>T | GRCh37 |
| NC_000001.9:g.97336742C>T | NCBI36 |
| NG_008807.2:g.827462G>A , LRG_722:g.827462G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370192.8:c.2657G>A (DPYD) MANE Select | ENSP00000359211.3:p.Arg886His | |
| ENST00000370192.7:c.2657G>A (DPYD) | ENSP00000359211.3:p.Arg886His | |
| NM_000110.3:c.2657G>A , LRG_722t1:c.2657G>A (DPYD) | NP_000101.2:p.Arg886His | |
| NR_046590.1:n.64+2612C>T (DPYD-AS1) | ||
| XM_005270562.3:c.2441G>A (DPYD) | XP_005270619.2:p.Arg814His | |
| XM_017000507.1:c.2546G>A (DPYD) | XP_016855996.1:p.Arg849His | |
| XM_017000508.2:c.2162G>A (DPYD) | XP_016855997.1:p.Arg721His | |
| XM_017000509.2:c.2162G>A (DPYD) | XP_016855998.1:p.Arg721His | |
| XM_017000510.1:c.2162G>A (DPYD) | XP_016855999.1:p.Arg721His | |
| NM_000110.4:c.2657G>A (DPYD) MANE Select | NP_000101.2:p.Arg886His |