Canonical Allele Identifier:
CA1681446562
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.170110297A= , CM000668.2:g.170110297A= | GRCh38 |
| NC_000006.11:g.170425521A= , CM000668.1:g.170425521A= | GRCh37 |
| NC_000006.10:g.170267446A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943319.1:n.566-2837T= | ||
| XR_943320.1:n.566-2837T= |