Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320786T= , CM000666.2:g.119320786T= | GRCh38 |
| NC_000004.11:g.120241941T= , CM000666.1:g.120241941T= | GRCh37 |
| NC_000004.10:g.120461389T= | NCBI36 |
| NG_011444.1:g.6376A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.124A= MANE Select | ENSP00000274024.3:p.Thr42= | |
| ENST00000274024.3:c.124A= | ENSP00000274024.3:p.Thr42= | |
| NM_000134.3:c.124A= | NP_000125.2:p.Thr42= | |
| NM_000134.4:c.124A= MANE Select | NP_000125.2:p.Thr42= |