Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153736726A= , CM000685.2:g.153736726A= | GRCh38 |
| NC_000023.10:g.153002180A= , CM000685.1:g.153002180A= | GRCh37 |
| NC_000023.9:g.152655374A= | NCBI36 |
| NG_009022.2:g.16859A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1393+213A= MANE Select | ENSP00000218104.3:n.1393+213A= | |
| ENST00000218104.5:c.1393+213A= | ENSP00000218104.3:n.1393+213A= | |
| ENST00000443684.2:n.396+213A= | ||
| NM_000033.3:c.1393+213A= | NP_000024.2:n.1393+213A= | |
| XR_938507.1:n.1810-130A= | ||
| XR_938507.2:n.1810-130A= | ||
| NM_000033.4:c.1393+213A= MANE Select | NP_000024.2:n.1393+213A= |