Canonical Allele Identifier:
CA2255112089
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237437T= , CM000679.2:g.30237437T= | GRCh38 |
| NC_000017.10:g.28564455T= , CM000679.1:g.28564455T= | GRCh37 |
| NC_000017.9:g.25588581T= | NCBI36 |
| NG_011747.2:g.3500A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.166-205T= | ||
| XR_001752824.1:n.281-205T= |