Canonical Allele Identifier:
CA15692951
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69819659G>A , CM000673.2:g.69819659G>A | GRCh38 |
| NC_000011.9:g.69634427G>A , CM000673.1:g.69634427G>A | GRCh37 |
| NC_000011.8:g.69343364G>A | NCBI36 |
| NG_009016.1:g.4766C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001748071.1:n.86+586G>A |