Canonical Allele Identifier:
CA2284239333
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.10321228T= , CM000680.2:g.10321228T= | GRCh38 |
| NC_000018.9:g.10321225T= , CM000680.1:g.10321225T= | GRCh37 |
| NC_000018.8:g.10311225T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935138.1:n.665+920A= | ||
| XR_001753344.1:n.650+920A= | ||
| XR_001753345.1:n.893A= | ||
| XR_001753346.1:n.549+920A= |