Canonical Allele Identifier:
CA2193611491
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.87166881T= , CM000677.2:g.87166881T= | GRCh38 |
| NC_000015.9:g.87710112T= , CM000677.1:g.87710112T= | GRCh37 |
| NC_000015.8:g.85511116T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_932582.1:n.167-11346T= | ||
| XR_932582.2:n.167-11346T= |