Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172986A= , CM000678.2:g.172986A= | GRCh38 |
| NC_000016.9:g.222985A= , CM000678.1:g.222985A= | GRCh37 |
| NC_000016.8:g.162985A= | NCBI36 |
| NG_000006.1:g.33849A= | |
| NG_059186.1:g.1336A= | |
| NG_059271.1:g.5140A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.74A= MANE Select | ENSP00000251595.6:p.Tyr25= | |
| ENST00000251595.10:c.74A= | ENSP00000251595.6:p.Tyr25= | |
| ENST00000397806.1:c.-2+28A= | ENSP00000380908.1:n.-2+28A= | |
| ENST00000482565.1:n.93A= | ||
| ENST00000484216.1:n.43A= | ||
| NM_000517.4:c.74A= | NP_000508.1:p.Tyr25= | |
| NM_000517.6:c.74A= MANE Select | NP_000508.1:p.Tyr25= |