Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764205A= , CM000674.2:g.57764205A= | GRCh38 |
| NC_000012.11:g.58157988A= , CM000674.1:g.58157988A= | GRCh37 |
| NC_000012.10:g.56444255A= | NCBI36 |
| NG_007076.1:g.7989T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000785.4:c.1137-29T= MANE Select | NP_000776.1:n.1137-29T= |
| ENST00000228606.9:c.1137-29T= MANE Select | ENSP00000228606.4:n.1137-29T= |
| NM_000785.3:c.1137-29T= | NP_000776.1:n.1137-29T= |
| ENST00000228606.8:c.1137-29T= | ENSP00000228606.4:n.1137-29T= |
| ENST00000546567.5:c.432-29T= | ENSP00000449472.1:n.432-29T= |
| ENST00000547344.5:n.1276-29T= | |
| ENST00000713544.1:c.1218-29T= | ENSP00000518840.1:n.1218-29T= |
| ENST00000713545.1:c.*142-29T= | ENSP00000518841.1:n.*142-29T= |