Canonical Allele Identifier:
CA1605276930
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.466005T= , CM000668.2:g.466005T= | GRCh38 |
| NC_000006.11:g.466005T= , CM000668.1:g.466005T= | GRCh37 |
| NC_000006.10:g.411005T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12280T= | ||
| XR_926365.1:n.2548+12280T= | ||
| XR_001743914.1:n.482-9203T= |