Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32220939A= , CM000668.2:g.32220939A= | GRCh38 |
| NC_000006.11:g.32188716A= , CM000668.1:g.32188716A= | GRCh37 |
| NC_000006.10:g.32296694A= | NCBI36 |
| NG_028190.1:g.8129T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.799+39T= MANE Select | ENSP00000364163.3:n.799+39T= | |
| ENST00000473562.1:n.928+39T= | ||
| NM_004557.3:c.799+39T= | NP_004548.3:n.799+39T= | |
| NR_134949.1:n.938+39T= | ||
| NR_134950.1:n.938+39T= | ||
| NM_004557.4:c.799+39T= MANE Select | NP_004548.3:n.799+39T= | |
| NR_134949.2:n.938+39T= | ||
| NR_134950.2:n.938+39T= |