Canonical Allele Identifier:
CA1605795032
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1535727A= , CM000668.2:g.1535727A= | GRCh38 |
| NC_000006.11:g.1535962A= , CM000668.1:g.1535962A= | GRCh37 |
| NC_000006.10:g.1480961A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_427861.2:n.234+16619T= | ||
| XR_926380.1:n.218-2729A= | ||
| XR_926381.1:n.1108-2729A= | ||
| XR_926382.1:n.235-6548T= | ||
| XR_926384.1:n.200-6548T= | ||
| XR_001743921.1:n.235-6572T= | ||
| XR_427861.3:n.234+16619T= | ||
| XR_926381.2:n.1123-2729A= |