Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172987T= , CM000678.2:g.172987T= | GRCh38 |
| NC_000016.9:g.222986T= , CM000678.1:g.222986T= | GRCh37 |
| NC_000016.8:g.162986T= | NCBI36 |
| NG_000006.1:g.33850T= | |
| NG_059186.1:g.1337T= | |
| NG_059271.1:g.5141T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.75T= MANE Select | NP_000508.1:p.Tyr25= |
| ENST00000251595.11:c.75T= MANE Select | ENSP00000251595.6:p.Tyr25= |
| NM_000517.4:c.75T= | NP_000508.1:p.Tyr25= |
| ENST00000251595.10:c.75T= | ENSP00000251595.6:p.Tyr25= |
| ENST00000397806.1:c.-2+29T= | ENSP00000380908.1:n.-2+29T= |
| ENST00000482565.1:n.94T= | |
| ENST00000484216.1:n.44T= |