Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785755G= , CM000681.2:g.18785755G= | GRCh38 |
| NC_000019.9:g.18896565G= , CM000681.1:g.18896565G= | GRCh37 |
| NC_000019.8:g.18757565G= | NCBI36 |
| NG_007070.1:g.10550C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1586C= MANE Select | ENSP00000222271.2:p.Thr529= | |
| ENST00000222271.6:c.1586C= | ENSP00000222271.2:p.Thr529= | |
| ENST00000425807.1:c.1427C= | ENSP00000403792.1:p.Thr476= | |
| ENST00000542601.6:c.1487C= | ENSP00000439156.2:p.Thr496= | |
| NM_000095.2:c.1586C= | NP_000086.2:p.Thr529= | |
| NM_000095.3:c.1586C= MANE Select | NP_000086.2:p.Thr529= |