Canonical Allele Identifier:
CA14152496
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.94775357C>T , CM000677.2:g.94775357C>T | GRCh38 |
| NC_000015.9:g.95318586C>T , CM000677.1:g.95318586C>T | GRCh37 |
| NC_000015.8:g.93119590C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932644.1:n.369-9340G>A | ||
| XR_932644.2:n.369-9340G>A |