Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47310917A= , CM000679.2:g.47310917A= | GRCh38 |
| NC_000017.10:g.45388283A= , CM000679.1:g.45388283A= | GRCh37 |
| NC_000017.9:g.42743282A= | NCBI36 |
| NG_008332.2:g.62076A= , LRG_481:g.62076A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000212.3:c.*713A= (ITGB3) MANE Select | NP_000203.2:n.*713A= |
| ENST00000559488.7:c.*713A= (ITGB3) MANE Select | ENSP00000452786.2:n.*713A= |
| NM_000212.2:c.*713A= , LRG_481t1:c.*713A= (ITGB3) | NP_000203.2:n.*713A= |
| NR_110880.1:n.363-7135T= (EFCAB13-DT) | |
| NR_110881.1:n.227-7135T= (EFCAB13-DT) | |
| ENST00000559488.5:c.*713A= (ITGB3) | ENSP00000452786.1:n.*713A= |
| ENST00000560629.1:c.2266+3280A= |