Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102066289C= , CM000672.2:g.102066289C= | GRCh38 |
| NC_000010.10:g.103826046C= , CM000672.1:g.103826046C= | GRCh37 |
| NC_000010.9:g.103816036C= | NCBI36 |
| NG_012029.1:g.5900C= , LRG_564:g.5900C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024747.6:c.815C= MANE Select | NP_079023.2:p.Thr272= |
| ENST00000299238.7:c.815C= MANE Select | ENSP00000299238.5:p.Thr272= |
| NM_024747.5:c.815C= , LRG_564t1:c.815C= | NP_079023.2:p.Thr272= |
| ENST00000299238.6:c.815C= | ENSP00000299238.5:p.Thr272= |