Canonical Allele Identifier:
CA1605795099
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1535892T= , CM000668.2:g.1535892T= | GRCh38 |
| NC_000006.11:g.1536127T= , CM000668.1:g.1536127T= | GRCh37 |
| NC_000006.10:g.1481126T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_427861.2:n.234+16454A= | ||
| XR_926380.1:n.218-2564T= | ||
| XR_926381.1:n.1108-2564T= | ||
| XR_926382.1:n.235-6713A= | ||
| XR_926384.1:n.200-6713A= | ||
| XR_001743921.1:n.235-6737A= | ||
| XR_427861.3:n.234+16454A= | ||
| XR_926381.2:n.1123-2564T= |