Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52516501A>G , CM000674.2:g.52516501A>G | GRCh38 |
| NC_000012.11:g.52910285A>G , CM000674.1:g.52910285A>G | GRCh37 |
| NC_000012.10:g.51196552A>G | NCBI36 |
| NG_008297.1:g.8959T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.1439+136T>C MANE Select | ENSP00000252242.4:n.1439+136T>C | |
| ENST00000252242.8:c.1439+136T>C | ENSP00000252242.4:n.1439+136T>C | |
| ENST00000548409.5:c.561+136T>C | ||
| ENST00000549511.5:n.646+136T>C | ||
| ENST00000552629.5:n.1673T>C | ||
| NM_000424.3:c.1439+136T>C | NP_000415.2:n.1439+136T>C | |
| NM_000424.4:c.1439+136T>C MANE Select | NP_000415.2:n.1439+136T>C |