Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319065T= , CM000673.2:g.6319065T= | GRCh38 |
| NC_000011.9:g.6340295T= , CM000673.1:g.6340295T= | GRCh37 |
| NC_000011.8:g.6296871T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*98A= MANE Select | ENSP00000307292.3:n.*98A= | |
| ENST00000303927.3:c.*98A= | ENSP00000307292.3:n.*98A= | |
| ENST00000532354.1:n.906A= | ||
| NM_145040.2:c.*98A= | NP_659477.2:n.*98A= | |
| XR_930997.1:n.720+845T= | ||
| NM_145040.3:c.*98A= MANE Select | NP_659477.2:n.*98A= |