Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110914203A= , CM000674.2:g.110914203A= | GRCh38 |
| NC_000012.11:g.111352007A= , CM000674.1:g.111352007A= | GRCh37 |
| NC_000012.10:g.109836390A= | NCBI36 |
| NG_007554.1:g.11375T= , LRG_393:g.11375T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000432.4:c.257T= MANE Select | NP_000423.2:p.Phe86= |
| ENST00000228841.15:c.257T= MANE Select | ENSP00000228841.8:p.Phe86= |
| NM_000432.3:c.257T= , LRG_393t1:c.257T= | NP_000423.2:p.Phe86= |
| ENST00000228841.12:c.257T= | ENSP00000228841.7:p.Phe86= |
| ENST00000548438.1:c.215T= | ENSP00000447154.1:p.Phe72= |
| ENST00000549029.1:n.88T= | |
| ENST00000663220.1:c.200T= | ENSP00000499568.1:p.Phe67= |