Linked Data
dbSNP Id:
rs752151811
ExAC:
1:97564096 T / G
gnomAD v2:
1-97564096-T-G
gnomAD v4:
1-97098540-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97098540T>G , CM000663.2:g.97098540T>G | GRCh38 |
| NC_000001.10:g.97564096T>G , CM000663.1:g.97564096T>G | GRCh37 |
| NC_000001.9:g.97336684T>G | NCBI36 |
| NG_008807.2:g.827520A>C , LRG_722:g.827520A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370192.8:c.2715A>C (DPYD) MANE Select | ENSP00000359211.3:p.Ser905= | |
| ENST00000370192.7:c.2715A>C (DPYD) | ENSP00000359211.3:p.Ser905= | |
| NM_000110.3:c.2715A>C , LRG_722t1:c.2715A>C (DPYD) | NP_000101.2:p.Ser905= | |
| NR_046590.1:n.64+2554T>G (DPYD-AS1) | ||
| XM_005270562.3:c.2499A>C (DPYD) | XP_005270619.2:p.Ser833= | |
| XM_017000507.1:c.2604A>C (DPYD) | XP_016855996.1:p.Ser868= | |
| XM_017000508.2:c.2220A>C (DPYD) | XP_016855997.1:p.Ser740= | |
| XM_017000509.2:c.2220A>C (DPYD) | XP_016855998.1:p.Ser740= | |
| XM_017000510.1:c.2220A>C (DPYD) | XP_016855999.1:p.Ser740= | |
| NM_000110.4:c.2715A>C (DPYD) MANE Select | NP_000101.2:p.Ser905= |