Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130209734G= , CM000673.2:g.130209734G= | GRCh38 |
| NC_000011.9:g.130079629G= , CM000673.1:g.130079629G= | GRCh37 |
| NC_000011.8:g.129584839G= | NCBI36 |
| NG_012132.1:g.54948G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021978.4:c.2479G= MANE Select | NP_068813.1:p.Gly827= |
| ENST00000278742.6:c.2479G= MANE Select | ENSP00000278742.5:p.Gly827= |
| NM_021978.3:c.2479G= | NP_068813.1:p.Gly827= |
| ENST00000278742.5:c.2479G= | ENSP00000278742.5:p.Gly827= |