Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173135T= , CM000678.2:g.173135T= | GRCh38 |
| NC_000016.9:g.223134T= , CM000678.1:g.223134T= | GRCh37 |
| NC_000016.8:g.163134T= | NCBI36 |
| NG_000006.1:g.33998T= | |
| NG_059186.1:g.1485T= | |
| NG_059271.1:g.5289T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.106T= MANE Select | NP_000508.1:p.Ser36= |
| ENST00000251595.11:c.106T= MANE Select | ENSP00000251595.6:p.Ser36= |
| NM_000517.4:c.106T= | NP_000508.1:p.Ser36= |
| ENST00000251595.10:c.106T= | ENSP00000251595.6:p.Ser36= |
| ENST00000397806.1:c.10T= | ENSP00000380908.1:p.Ser4= |
| ENST00000482565.1:n.242T= | |
| ENST00000484216.1:n.75T= |