Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14197151T= , CM000673.2:g.14197151T= | GRCh38 |
| NC_000011.9:g.14218697T= , CM000673.1:g.14218697T= | GRCh37 |
| NC_000011.8:g.14175273T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000576479.4:c.826-46181T= MANE Select | ENSP00000460236.1:n.826-46181T= | |
| ENST00000576479.3:c.826-46181T= | ENSP00000460236.1:n.826-46181T= | |
| NM_006108.3:c.826-46181T= | NP_006099.2:n.826-46181T= | |
| NM_006108.4:c.826-46181T= MANE Select | NP_006099.2:n.826-46181T= |