Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57765111C= , CM000674.2:g.57765111C= | GRCh38 |
| NC_000012.11:g.58158894C= , CM000674.1:g.58158894C= | GRCh37 |
| NC_000012.10:g.56445161C= | NCBI36 |
| NG_007076.1:g.7083G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000546609.2:n.602G= | ||
| ENST00000713544.1:c.771G= | ENSP00000518840.1:p.Val257= | |
| ENST00000713545.1:c.748G= | ENSP00000518841.1:p.Val250= | |
| ENST00000228606.9:c.690G= MANE Select | ENSP00000228606.4:p.Val230= | |
| ENST00000228606.8:c.690G= | ENSP00000228606.4:p.Val230= | |
| ENST00000546567.5:c.-16G= | ENSP00000449472.1:n.-16G= | |
| ENST00000546609.1:c.602G= | ||
| ENST00000547344.5:n.829G= | ||
| ENST00000547451.1:n.490G= | ||
| NM_000785.3:c.690G= | NP_000776.1:p.Val230= | |
| NM_000785.4:c.690G= MANE Select | NP_000776.1:p.Val230= |