Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172982G= , CM000678.2:g.172982G= | GRCh38 |
| NC_000016.9:g.222981G= , CM000678.1:g.222981G= | GRCh37 |
| NC_000016.8:g.162981G= | NCBI36 |
| NG_000006.1:g.33845G= | |
| NG_059186.1:g.1332G= | |
| NG_059271.1:g.5136G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.70G= MANE Select | NP_000508.1:p.Glu24= |
| ENST00000251595.11:c.70G= MANE Select | ENSP00000251595.6:p.Glu24= |
| NM_000517.4:c.70G= | NP_000508.1:p.Glu24= |
| ENST00000251595.10:c.70G= | ENSP00000251595.6:p.Glu24= |
| ENST00000397806.1:c.-2+24G= | ENSP00000380908.1:n.-2+24G= |
| ENST00000482565.1:n.89G= | |
| ENST00000484216.1:n.39G= |