Canonical Allele Identifier:
CA1687788335
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.10667285T= , CM000669.2:g.10667285T= | GRCh38 |
| NC_000007.13:g.10706912T= , CM000669.1:g.10706912T= | GRCh37 |
| NC_000007.12:g.10673437T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_147499.1:n.64-105708A= | |
| XR_001745090.1:n.376-8011T= |