Linked Data
dbSNP Id:
rs761609256
ExAC:
1:97700439 T / G
gnomAD v2:
1-97700439-T-G
gnomAD v4:
1-97234883-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97234883T>G , CM000663.2:g.97234883T>G | GRCh38 |
| NC_000001.10:g.97700439T>G , CM000663.1:g.97700439T>G | GRCh37 |
| NC_000001.9:g.97473027T>G | NCBI36 |
| NG_008807.2:g.691177A>C , LRG_722:g.691177A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370192.8:c.2411A>C (DPYD) MANE Select | ENSP00000359211.3:p.Gln804Pro | |
| ENST00000370192.7:c.2411A>C (DPYD) | ENSP00000359211.3:p.Gln804Pro | |
| NM_000110.3:c.2411A>C , LRG_722t1:c.2411A>C (DPYD) | NP_000101.2:p.Gln804Pro | |
| NR_046590.1:n.65-30531T>G (DPYD-AS1) | ||
| XM_005270562.3:c.2195A>C (DPYD) | XP_005270619.2:p.Gln732Pro | |
| XM_006710397.2:c.2411A>C (DPYD) | XP_006710460.1:p.Gln804Pro | |
| XM_006710397.3:c.2411A>C (DPYD) | XP_006710460.1:p.Gln804Pro | |
| XM_017000507.1:c.2300A>C (DPYD) | XP_016855996.1:p.Gln767Pro | |
| XM_017000508.2:c.1916A>C (DPYD) | XP_016855997.1:p.Gln639Pro | |
| XM_017000509.2:c.1916A>C (DPYD) | XP_016855998.1:p.Gln639Pro | |
| XM_017000510.1:c.1916A>C (DPYD) | XP_016855999.1:p.Gln639Pro | |
| NM_000110.4:c.2411A>C (DPYD) MANE Select | NP_000101.2:p.Gln804Pro |