Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319125C= , CM000673.2:g.6319125C= | GRCh38 |
| NC_000011.9:g.6340355C= , CM000673.1:g.6340355C= | GRCh37 |
| NC_000011.8:g.6296931C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*38G= MANE Select | ENSP00000307292.3:n.*38G= | |
| ENST00000303927.3:c.*38G= | ENSP00000307292.3:n.*38G= | |
| ENST00000532354.1:n.846G= | ||
| NM_145040.2:c.*38G= | NP_659477.2:n.*38G= | |
| XR_930997.1:n.720+905C= | ||
| NM_145040.3:c.*38G= MANE Select | NP_659477.2:n.*38G= |