Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431326T= , CM000663.2:g.68431326T= | GRCh38 |
| NC_000001.10:g.68897009T= , CM000663.1:g.68897009T= | GRCh37 |
| NC_000001.9:g.68669597T= | NCBI36 |
| NG_008472.1:g.23634A= | |
| NG_008472.2:g.23634A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1294A= MANE Select | ENSP00000262340.5:p.Thr432= | |
| ENST00000262340.5:c.1294A= | ENSP00000262340.5:p.Thr432= | |
| NM_000329.2:c.1294A= | NP_000320.1:p.Thr432= | |
| XM_017002027.1:c.1018A= | XP_016857516.1:p.Thr340= | |
| NM_000329.3:c.1294A= MANE Select | NP_000320.1:p.Thr432= |