Linked Data
dbSNP Id:
rs773002572
ExAC:
1:97564165 A / G
gnomAD v2:
1-97564165-A-G
gnomAD v3:
1-97098609-A-G
gnomAD v4:
1-97098609-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97098609A>G , CM000663.2:g.97098609A>G | GRCh38 |
| NC_000001.10:g.97564165A>G , CM000663.1:g.97564165A>G | GRCh37 |
| NC_000001.9:g.97336753A>G | NCBI36 |
| NG_008807.2:g.827451T>C , LRG_722:g.827451T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370192.8:c.2646T>C (DPYD) MANE Select | ENSP00000359211.3:p.Tyr882= | |
| ENST00000370192.7:c.2646T>C (DPYD) | ENSP00000359211.3:p.Tyr882= | |
| NM_000110.3:c.2646T>C , LRG_722t1:c.2646T>C (DPYD) | NP_000101.2:p.Tyr882= | |
| NR_046590.1:n.64+2623A>G (DPYD-AS1) | ||
| XM_005270562.3:c.2430T>C (DPYD) | XP_005270619.2:p.Tyr810= | |
| XM_017000507.1:c.2535T>C (DPYD) | XP_016855996.1:p.Tyr845= | |
| XM_017000508.2:c.2151T>C (DPYD) | XP_016855997.1:p.Tyr717= | |
| XM_017000509.2:c.2151T>C (DPYD) | XP_016855998.1:p.Tyr717= | |
| XM_017000510.1:c.2151T>C (DPYD) | XP_016855999.1:p.Tyr717= | |
| NM_000110.4:c.2646T>C (DPYD) MANE Select | NP_000101.2:p.Tyr882= |