Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.76347214C= , CM000674.2:g.76347214C= | GRCh38 |
| NC_000012.11:g.76740994C= , CM000674.1:g.76740994C= | GRCh37 |
| NC_000012.10:g.75265125C= | NCBI36 |
| NG_016357.1:g.6229G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650064.2:c.771G= MANE Select | ENSP00000497413.1:p.Met257= | |
| ENST00000393262.3:c.771G= | ENSP00000376946.3:p.Met257= | |
| NM_024685.3:c.771G= | NP_078961.3:p.Met257= | |
| NM_024685.4:c.771G= MANE Select | NP_078961.3:p.Met257= |