Linked Data
dbSNP Id:
rs963318212
gnomAD v2:
1-97770833-T-C
gnomAD v3:
1-97305277-T-C
gnomAD v4:
1-97305277-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97305277T>C , CM000663.2:g.97305277T>C | GRCh38 |
| NC_000001.10:g.97770833T>C , CM000663.1:g.97770833T>C | GRCh37 |
| NC_000001.9:g.97543421T>C | NCBI36 |
| NG_008807.2:g.620783A>G , LRG_722:g.620783A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370192.8:c.2281A>G (DPYD) MANE Select | ENSP00000359211.3:p.Thr761Ala | |
| ENST00000370192.7:c.2281A>G (DPYD) | ENSP00000359211.3:p.Thr761Ala | |
| NM_000110.3:c.2281A>G , LRG_722t1:c.2281A>G (DPYD) | NP_000101.2:p.Thr761Ala | |
| NR_046590.1:n.129-912T>C (DPYD-AS1) | ||
| XM_005270562.3:c.2065A>G (DPYD) | XP_005270619.2:p.Thr689Ala | |
| XM_006710397.2:c.2281A>G (DPYD) | XP_006710460.1:p.Thr761Ala | |
| XM_006710397.3:c.2281A>G (DPYD) | XP_006710460.1:p.Thr761Ala | |
| XM_017000507.1:c.2170A>G (DPYD) | XP_016855996.1:p.Thr724Ala | |
| XM_017000508.2:c.1786A>G (DPYD) | XP_016855997.1:p.Thr596Ala | |
| XM_017000509.2:c.1786A>G (DPYD) | XP_016855998.1:p.Thr596Ala | |
| XM_017000510.1:c.1786A>G (DPYD) | XP_016855999.1:p.Thr596Ala | |
| NM_000110.4:c.2281A>G (DPYD) MANE Select | NP_000101.2:p.Thr761Ala |