Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94965778A= , CM000672.2:g.94965778A= | GRCh38 |
| NC_000010.10:g.96725535A= , CM000672.1:g.96725535A= | GRCh37 |
| NC_000010.9:g.96715525A= | NCBI36 |
| NG_008385.1:g.32121A= | |
| NG_008385.2:g.32621A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000771.4:c.820-6326A= MANE Select | NP_000762.2:n.820-6326A= |
| ENST00000260682.8:c.820-6326A= MANE Select | ENSP00000260682.6:n.820-6326A= |
| NM_000771.3:c.820-6326A= | NP_000762.2:n.820-6326A= |
| ENST00000260682.6:c.820-6326A= | ENSP00000260682.6:n.820-6326A= |
| ENST00000643112.1:c.820-15405A= | ENSP00000496202.1:n.820-15405A= |