Linked Data
dbSNP Id:
rs11587873
gnomAD v2:
1-97653070-C-T
gnomAD v3:
1-97187514-C-T
gnomAD v4:
1-97187514-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97187514C>T , CM000663.2:g.97187514C>T | GRCh38 |
| NC_000001.10:g.97653070C>T , CM000663.1:g.97653070C>T | GRCh37 |
| NC_000001.9:g.97425658C>T | NCBI36 |
| NG_008807.2:g.738546G>A , LRG_722:g.738546G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370192.8:c.2622+5555G>A (DPYD) MANE Select | ENSP00000359211.3:n.2622+5555G>A | |
| ENST00000370192.7:c.2622+5555G>A (DPYD) | ENSP00000359211.3:n.2622+5555G>A | |
| NM_000110.3:c.2622+5555G>A , LRG_722t1:c.2622+5555G>A (DPYD) | NP_000101.2:n.2622+5555G>A | |
| NR_046590.1:n.65-77900C>T (DPYD-AS1) | ||
| XM_005270562.3:c.2406+5555G>A (DPYD) | XP_005270619.2:n.2406+5555G>A | |
| XM_017000507.1:c.2511+5555G>A (DPYD) | XP_016855996.1:n.2511+5555G>A | |
| XM_017000508.2:c.2127+5555G>A (DPYD) | XP_016855997.1:n.2127+5555G>A | |
| XM_017000509.2:c.2127+5555G>A (DPYD) | XP_016855998.1:n.2127+5555G>A | |
| XM_017000510.1:c.2127+5555G>A (DPYD) | XP_016855999.1:n.2127+5555G>A | |
| NM_000110.4:c.2622+5555G>A (DPYD) MANE Select | NP_000101.2:n.2622+5555G>A |