Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133536297T= , CM000672.2:g.133536297T= | GRCh38 |
| NC_000010.10:g.135349801T= , CM000672.1:g.135349801T= | GRCh37 |
| NC_000010.9:g.135199791T= | NCBI36 |
| NG_008383.1:g.13935T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000773.4:c.968-766T= MANE Select | NP_000764.1:n.968-766T= |
| ENST00000252945.8:c.968-766T= MANE Select | ENSP00000252945.3:n.968-766T= |
| NM_000773.3:c.968-766T= | NP_000764.1:n.968-766T= |
| ENST00000252945.7:c.968-766T= | ENSP00000252945.3:n.968-766T= |
| ENST00000368520.1:n.1029-766T= | |
| ENST00000418356.1:c.557-766T= | ENSP00000397299.1:n.557-766T= |
| ENST00000421586.5:c.707-766T= | ENSP00000412754.1:n.707-766T= |
| ENST00000463117.6:c.968-766T= | ENSP00000440689.1:n.968-766T= |
| ENST00000541080.5:c.384-766T= |