Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173128G= , CM000678.2:g.173128G= | GRCh38 |
| NC_000016.9:g.223127G= , CM000678.1:g.223127G= | GRCh37 |
| NC_000016.8:g.163127G= | NCBI36 |
| NG_000006.1:g.33991G= | |
| NG_059186.1:g.1478G= | |
| NG_059271.1:g.5282G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.99G= MANE Select | NP_000508.1:p.Met33= |
| ENST00000251595.11:c.99G= MANE Select | ENSP00000251595.6:p.Met33= |
| NM_000517.4:c.99G= | NP_000508.1:p.Met33= |
| ENST00000251595.10:c.99G= | ENSP00000251595.6:p.Met33= |
| ENST00000397806.1:c.3G= | ENSP00000380908.1:p.Met1= |
| ENST00000482565.1:n.235G= | |
| ENST00000484216.1:n.68G= |