Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47310191A>C , CM000679.2:g.47310191A>C | GRCh38 |
| NC_000017.10:g.45387557A>C , CM000679.1:g.45387557A>C | GRCh37 |
| NC_000017.9:g.42742556A>C | NCBI36 |
| NG_008332.2:g.61350A>C , LRG_481:g.61350A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559488.7:c.2354A>C (ITGB3) MANE Select | ENSP00000452786.2:p.Tyr785Ser | |
| ENST00000559488.5:c.2354A>C (ITGB3) | ENSP00000452786.1:p.Tyr785Ser | |
| ENST00000560629.1:c.2266+2554A>C | ||
| NM_000212.2:c.2354A>C , LRG_481t1:c.2354A>C (ITGB3) | NP_000203.2:p.Tyr785Ser | |
| NR_110880.1:n.363-6409T>G (EFCAB13-DT) | ||
| NR_110881.1:n.227-6409T>G (EFCAB13-DT) | ||
| NM_000212.3:c.2354A>C (ITGB3) MANE Select | NP_000203.2:p.Tyr785Ser |