Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4370383G= , CM000674.2:g.4370383G= | GRCh38 |
| NC_000012.11:g.4479549G= , CM000674.1:g.4479549G= | GRCh37 |
| NC_000012.10:g.4349810G= | NCBI36 |
| NG_007087.1:g.14346C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020638.3:c.716C= MANE Select | NP_065689.1:p.Thr239= |
| ENST00000237837.2:c.716C= MANE Select | ENSP00000237837.1:p.Thr239= |
| NM_020638.2:c.716C= | NP_065689.1:p.Thr239= |
| ENST00000237837.1:c.716C= | ENSP00000237837.1:p.Thr239= |
| ENST00000648100.1:c.*1967+4101G= | ENSP00000497536.1:n.*1967+4101G= |
| ENST00000674624.1:c.*1204+4101G= | ENSP00000501898.1:n.*1204+4101G= |