Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763850T= , CM000674.2:g.57763850T= | GRCh38 |
| NC_000012.11:g.58157633T= , CM000674.1:g.58157633T= | GRCh37 |
| NC_000012.10:g.56443900T= | NCBI36 |
| NG_007076.1:g.8344A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1297-42A= | ENSP00000518840.1:n.1297-42A= | |
| ENST00000713545.1:c.*221-42A= | ENSP00000518841.1:n.*221-42A= | |
| ENST00000228606.9:c.1216-42A= MANE Select | ENSP00000228606.4:n.1216-42A= | |
| ENST00000228606.8:c.1216-42A= | ENSP00000228606.4:n.1216-42A= | |
| ENST00000547344.5:n.1355-42A= | ||
| NM_000785.3:c.1216-42A= | NP_000776.1:n.1216-42A= | |
| NM_000785.4:c.1216-42A= MANE Select | NP_000776.1:n.1216-42A= |