Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.125956807G= , CM000673.2:g.125956807G= | GRCh38 |
| NC_000011.9:g.125826702G= , CM000673.1:g.125826702G= | GRCh37 |
| NC_000011.8:g.125331912G= | NCBI36 |
| NG_029776.1:g.111486C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000392693.7:c.*4135C= (CDON) | ENSP00000376458.3:n.*4135C= |
| ENST00000638636.2:c.3197G= (VSIG10L2) | ENSP00000491467.1:n.3197G= |
| ENST00000684078.1:c.*4135C= (CDON) | ENSP00000507318.1:n.*4135C= |
| XM_006718950.2:c.3593G= (VSIG10L2) | XP_006719013.2:n.3593G= |