Linked Data
dbSNP Id:
rs1411946304
gnomAD v2:
1-97700497-G-T
gnomAD v3:
1-97234941-G-T
gnomAD v4:
1-97234941-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97234941G>T , CM000663.2:g.97234941G>T | GRCh38 |
| NC_000001.10:g.97700497G>T , CM000663.1:g.97700497G>T | GRCh37 |
| NC_000001.9:g.97473085G>T | NCBI36 |
| NG_008807.2:g.691119C>A , LRG_722:g.691119C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370192.8:c.2353C>A (DPYD) MANE Select | ENSP00000359211.3:p.Leu785Met | |
| ENST00000370192.7:c.2353C>A (DPYD) | ENSP00000359211.3:p.Leu785Met | |
| NM_000110.3:c.2353C>A , LRG_722t1:c.2353C>A (DPYD) | NP_000101.2:p.Leu785Met | |
| NR_046590.1:n.65-30473G>T (DPYD-AS1) | ||
| XM_005270562.3:c.2137C>A (DPYD) | XP_005270619.2:p.Leu713Met | |
| XM_006710397.2:c.2353C>A (DPYD) | XP_006710460.1:p.Leu785Met | |
| XM_006710397.3:c.2353C>A (DPYD) | XP_006710460.1:p.Leu785Met | |
| XM_017000507.1:c.2242C>A (DPYD) | XP_016855996.1:p.Leu748Met | |
| XM_017000508.2:c.1858C>A (DPYD) | XP_016855997.1:p.Leu620Met | |
| XM_017000509.2:c.1858C>A (DPYD) | XP_016855998.1:p.Leu620Met | |
| XM_017000510.1:c.1858C>A (DPYD) | XP_016855999.1:p.Leu620Met | |
| NM_000110.4:c.2353C>A (DPYD) MANE Select | NP_000101.2:p.Leu785Met |