Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.147830478A= , CM000667.2:g.147830478A= | GRCh38 |
| NC_000005.9:g.147210041A= , CM000667.1:g.147210041A= | GRCh37 |
| NC_000005.8:g.147190234A= | NCBI36 |
| NG_008356.2:g.13754T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296695.10:c.56-848T= MANE Select | ENSP00000296695.5:n.56-848T= | |
| ENST00000296695.9:c.56-848T= | ENSP00000296695.5:n.56-848T= | |
| ENST00000510027.2:c.56-848T= | ENSP00000427376.1:n.56-848T= | |
| NM_003122.4:c.56-848T= | NP_003113.2:n.56-848T= | |
| NM_001354966.1:c.56-848T= | NP_001341895.1:n.56-848T= | |
| NM_001354966.2:c.56-848T= | NP_001341895.1:n.56-848T= | |
| NM_001379610.1:c.56-848T= MANE Select | NP_001366539.1:n.56-848T= | |
| NM_003122.5:c.56-848T= | NP_003113.2:n.56-848T= |