Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766131C= , CM000674.2:g.57766131C= | GRCh38 |
| NC_000012.11:g.58159914C= , CM000674.1:g.58159914C= | GRCh37 |
| NC_000012.10:g.56446181C= | NCBI36 |
| NG_007076.1:g.6063G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000785.4:c.262G= MANE Select | NP_000776.1:p.Val88= |
| ENST00000228606.9:c.262G= MANE Select | ENSP00000228606.4:p.Val88= |
| NM_000785.3:c.262G= | NP_000776.1:p.Val88= |
| ENST00000228606.8:c.262G= | ENSP00000228606.4:p.Val88= |
| ENST00000546496.1:n.90G= | |
| ENST00000546609.1:c.174G= | |
| ENST00000546609.2:n.174G= | |
| ENST00000547344.5:n.316G= | |
| ENST00000552186.1:n.381G= | |
| ENST00000713544.1:c.262G= | ENSP00000518840.1:p.Val88= |
| ENST00000713545.1:c.262G= | ENSP00000518841.1:p.Val88= |