Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52517702A= , CM000674.2:g.52517702A= | GRCh38 |
| NC_000012.11:g.52911486A= , CM000674.1:g.52911486A= | GRCh37 |
| NC_000012.10:g.51197753A= | NCBI36 |
| NG_008297.1:g.7758T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000424.4:c.980T= MANE Select | NP_000415.2:p.Met327= |
| ENST00000252242.9:c.980T= MANE Select | ENSP00000252242.4:p.Met327= |
| NM_000424.3:c.980T= | NP_000415.2:p.Met327= |
| ENST00000252242.8:c.980T= | ENSP00000252242.4:p.Met327= |
| ENST00000547890.5:n.109T= | |
| ENST00000548409.5:c.102T= | |
| ENST00000549511.5:n.187T= | |
| ENST00000551013.1:n.618T= | |
| ENST00000551188.5:c.423T= | |
| ENST00000552629.5:n.1078T= |