Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52516665G= , CM000674.2:g.52516665G= | GRCh38 |
| NC_000012.11:g.52910449G= , CM000674.1:g.52910449G= | GRCh37 |
| NC_000012.10:g.51196716G= | NCBI36 |
| NG_008297.1:g.8795C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000424.4:c.1411C= MANE Select | NP_000415.2:p.Arg471= |
| ENST00000252242.9:c.1411C= MANE Select | ENSP00000252242.4:p.Arg471= |
| NM_000424.3:c.1411C= | NP_000415.2:p.Arg471= |
| ENST00000252242.8:c.1411C= | ENSP00000252242.4:p.Arg471= |
| ENST00000548409.5:c.533C= | |
| ENST00000549511.5:n.618C= | |
| ENST00000552629.5:n.1509C= |