Linked Data
dbSNP Id:
rs139543981
gnomAD v2:
1-97770921-G-T
gnomAD v3:
1-97305365-G-T
gnomAD v4:
1-97305365-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97305365G>T , CM000663.2:g.97305365G>T | GRCh38 |
| NC_000001.10:g.97770921G>T , CM000663.1:g.97770921G>T | GRCh37 |
| NC_000001.9:g.97543509G>T | NCBI36 |
| NG_008807.2:g.620695C>A , LRG_722:g.620695C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370192.8:c.2193C>A (DPYD) MANE Select | ENSP00000359211.3:p.Gly731= | |
| ENST00000370192.7:c.2193C>A (DPYD) | ENSP00000359211.3:p.Gly731= | |
| NM_000110.3:c.2193C>A , LRG_722t1:c.2193C>A (DPYD) | NP_000101.2:p.Gly731= | |
| NR_046590.1:n.129-824G>T (DPYD-AS1) | ||
| XM_005270562.3:c.1977C>A (DPYD) | XP_005270619.2:p.Gly659= | |
| XM_006710397.2:c.2193C>A (DPYD) | XP_006710460.1:p.Gly731= | |
| XM_006710397.3:c.2193C>A (DPYD) | XP_006710460.1:p.Gly731= | |
| XM_017000507.1:c.2082C>A (DPYD) | XP_016855996.1:p.Gly694= | |
| XM_017000508.2:c.1698C>A (DPYD) | XP_016855997.1:p.Gly566= | |
| XM_017000509.2:c.1698C>A (DPYD) | XP_016855998.1:p.Gly566= | |
| XM_017000510.1:c.1698C>A (DPYD) | XP_016855999.1:p.Gly566= | |
| NM_000110.4:c.2193C>A (DPYD) MANE Select | NP_000101.2:p.Gly731= |