Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70176238C= , CM000679.2:g.70176238C= | GRCh38 |
| NC_000017.10:g.68172379C= , CM000679.1:g.68172379C= | GRCh37 |
| NC_000017.9:g.65683974C= | NCBI36 |
| NG_008798.1:g.11704C= , LRG_328:g.11704C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000891.3:c.1199C= MANE Select | NP_000882.1:p.Thr400= |
| ENST00000243457.4:c.1199C= MANE Select | ENSP00000243457.2:p.Thr400= |
| NM_000891.2:c.1199C= , LRG_328t1:c.1199C= | NP_000882.1:p.Thr400= |
| ENST00000243457.3:c.1199C= | ENSP00000243457.2:p.Thr400= |
| ENST00000535240.1:c.1199C= | ENSP00000441848.1:p.Thr400= |
| XM_011524779.1:c.1199C= | XP_011523081.1:p.Thr400= |