Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7743430G= , CM000668.2:g.7743430G= | GRCh38 |
| NC_000006.11:g.7743663G= , CM000668.1:g.7743663G= | GRCh37 |
| NC_000006.10:g.7688662G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283147.7:c.664+15811G= MANE Select | ENSP00000283147.6:n.664+15811G= | |
| ENST00000283147.6:c.664+15811G= | ENSP00000283147.6:n.664+15811G= | |
| NM_001718.4:c.664+15811G= | NP_001709.1:n.664+15811G= | |
| NM_001718.5:c.664+15811G= | NP_001709.1:n.664+15811G= | |
| NM_001718.6:c.664+15811G= MANE Select | NP_001709.1:n.664+15811G= |