Canonical Allele Identifier:
CA1609069970
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.8525236T= , CM000668.2:g.8525236T= | GRCh38 |
| NC_000006.11:g.8525469T= , CM000668.1:g.8525469T= | GRCh37 |
| NC_000006.10:g.8470468T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_038979.1:n.626-33349T= | ||
| NR_038980.1:n.649-33349T= |