Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051613T= , CM000675.2:g.53051613T= | GRCh38 |
| NC_000013.10:g.53625748T= , CM000675.1:g.53625748T= | GRCh37 |
| NC_000013.9:g.52523749T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219022.3:c.*842T= MANE Select | ENSP00000219022.2:n.*842T= | |
| ENST00000219022.2:c.*842T= | ENSP00000219022.2:n.*842T= | |
| NM_006418.4:c.*842T= | NP_006409.3:n.*842T= | |
| NM_006418.5:c.*842T= MANE Select | NP_006409.3:n.*842T= |