Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107683367T= , CM000669.2:g.107683367T= | GRCh38 |
| NC_000007.13:g.107323812T= , CM000669.1:g.107323812T= | GRCh37 |
| NC_000007.12:g.107111048T= | NCBI36 |
| NG_008489.1:g.27733T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.918+13T= MANE Select | ENSP00000494017.1:n.918+13T= | |
| ENST00000265715.7:c.918+13T= | ENSP00000265715.3:n.918+13T= | |
| NM_000441.1:c.918+13T= | NP_000432.1:n.918+13T= | |
| XM_005250425.1:c.918+13T= | XP_005250482.1:n.918+13T= | |
| XM_006716025.2:c.918+13T= | XP_006716088.1:n.918+13T= | |
| XM_005250425.2:c.918+13T= | XP_005250482.1:n.918+13T= | |
| XM_006716025.3:c.918+13T= | XP_006716088.1:n.918+13T= | |
| XM_017012318.1:c.918+13T= | XP_016867807.1:n.918+13T= | |
| NM_000441.2:c.918+13T= MANE Select | NP_000432.1:n.918+13T= |