Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763849A= , CM000674.2:g.57763849A= | GRCh38 |
| NC_000012.11:g.58157632A= , CM000674.1:g.58157632A= | GRCh37 |
| NC_000012.10:g.56443899A= | NCBI36 |
| NG_007076.1:g.8345T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1297-41T= | ENSP00000518840.1:n.1297-41T= | |
| ENST00000713545.1:c.*221-41T= | ENSP00000518841.1:n.*221-41T= | |
| ENST00000228606.9:c.1216-41T= MANE Select | ENSP00000228606.4:n.1216-41T= | |
| ENST00000228606.8:c.1216-41T= | ENSP00000228606.4:n.1216-41T= | |
| ENST00000547344.5:n.1355-41T= | ||
| NM_000785.3:c.1216-41T= | NP_000776.1:n.1216-41T= | |
| NM_000785.4:c.1216-41T= MANE Select | NP_000776.1:n.1216-41T= |