Canonical Allele Identifier:
CA2136398902
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50856969T= , CM000676.2:g.50856969T= | GRCh38 |
| NC_000014.8:g.51323687T= , CM000676.1:g.51323687T= | GRCh37 |
| NC_000014.7:g.50393437T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_943848.1:n.282+1129A= | ||
| XR_943848.2:n.643+1129A= |