Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173503C= , CM000678.2:g.173503C= | GRCh38 |
| NC_000016.9:g.223502C= , CM000678.1:g.223502C= | GRCh37 |
| NC_000016.8:g.163502C= | NCBI36 |
| NG_000006.1:g.34366C= | |
| NG_059186.1:g.1853C= | |
| NG_059271.1:g.5657C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.332C= MANE Select | NP_000508.1:p.Ala111= |
| ENST00000251595.11:c.332C= MANE Select | ENSP00000251595.6:p.Ala111= |
| NM_000517.4:c.332C= | NP_000508.1:p.Ala111= |
| ENST00000251595.10:c.332C= | ENSP00000251595.6:p.Ala111= |
| ENST00000397806.1:c.236C= | ENSP00000380908.1:p.Ala79= |
| ENST00000482565.1:n.468C= |