Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7881078A= , CM000668.2:g.7881078A= | GRCh38 |
| NC_000006.11:g.7881311A= , CM000668.1:g.7881311A= | GRCh37 |
| NC_000006.10:g.7826310A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001718.6:c.*735A= MANE Select | NP_001709.1:n.*735A= |
| ENST00000283147.7:c.*735A= MANE Select | ENSP00000283147.6:n.*735A= |
| NM_001718.4:c.*735A= | NP_001709.1:n.*735A= |
| NM_001718.5:c.*735A= | NP_001709.1:n.*735A= |
| ENST00000283147.6:c.*735A= | ENSP00000283147.6:n.*735A= |