Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.34855410T= , CM000668.2:g.34855410T= | GRCh38 |
| NC_000006.11:g.34823187T= , CM000668.1:g.34823187T= | GRCh37 |
| NC_000006.10:g.34931165T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000192788.6:c.1034-207T= MANE Select | ENSP00000192788.5:n.1034-207T= | |
| ENST00000192788.5:c.1034-207T= | ENSP00000192788.5:n.1034-207T= | |
| ENST00000452449.6:c.1034-207T= | ENSP00000400628.2:n.1034-207T= | |
| NM_017754.3:c.1034-207T= | NP_060224.3:n.1034-207T= | |
| XM_006715126.2:c.1034-207T= | XP_006715189.1:n.1034-207T= | |
| XM_011514714.1:c.1034-829T= | XP_011513016.1:n.1034-829T= | |
| XM_011514715.1:c.38-207T= | XP_011513017.1:n.38-207T= | |
| NM_017754.4:c.1034-207T= MANE Select | NP_060224.3:n.1034-207T= |