Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173009T= , CM000678.2:g.173009T= | GRCh38 |
| NC_000016.9:g.223008T= , CM000678.1:g.223008T= | GRCh37 |
| NC_000016.8:g.163008T= | NCBI36 |
| NG_000006.1:g.33872T= | |
| NG_059186.1:g.1359T= | |
| NG_059271.1:g.5163T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.95+2T= MANE Select | ENSP00000251595.6:n.95+2T= | |
| ENST00000251595.10:c.95+2T= | ENSP00000251595.6:n.95+2T= | |
| ENST00000397806.1:c.-2+51T= | ENSP00000380908.1:n.-2+51T= | |
| ENST00000482565.1:n.116T= | ||
| ENST00000484216.1:n.64+2T= | ||
| NM_000517.4:c.95+2T= | NP_000508.1:n.95+2T= | |
| NM_000517.6:c.95+2T= MANE Select | NP_000508.1:n.95+2T= |