Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172981C= , CM000678.2:g.172981C= | GRCh38 |
| NC_000016.9:g.222980C= , CM000678.1:g.222980C= | GRCh37 |
| NC_000016.8:g.162980C= | NCBI36 |
| NG_000006.1:g.33844C= | |
| NG_059186.1:g.1331C= | |
| NG_059271.1:g.5135C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.69C= MANE Select | NP_000508.1:p.Gly23= |
| ENST00000251595.11:c.69C= MANE Select | ENSP00000251595.6:p.Gly23= |
| NM_000517.4:c.69C= | NP_000508.1:p.Gly23= |
| ENST00000251595.10:c.69C= | ENSP00000251595.6:p.Gly23= |
| ENST00000397806.1:c.-2+23C= | ENSP00000380908.1:n.-2+23C= |
| ENST00000482565.1:n.88C= | |
| ENST00000484216.1:n.38C= |