Canonical Allele Identifier:
CA1768678649
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19225642C= , CM000670.2:g.19225642C= | GRCh38 |
| NC_000008.10:g.19083152C= , CM000670.1:g.19083152C= | GRCh37 |
| NC_000008.9:g.19127432C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_038919.1:n.568+1526G= |