Canonical Allele Identifier:
CA1605795049
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1535771G= , CM000668.2:g.1535771G= | GRCh38 |
| NC_000006.11:g.1536006G= , CM000668.1:g.1536006G= | GRCh37 |
| NC_000006.10:g.1481005G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_427861.2:n.234+16575C= | ||
| XR_926380.1:n.218-2685G= | ||
| XR_926381.1:n.1108-2685G= | ||
| XR_926382.1:n.235-6592C= | ||
| XR_926384.1:n.200-6592C= | ||
| XR_001743921.1:n.235-6616C= | ||
| XR_427861.3:n.234+16575C= | ||
| XR_926381.2:n.1123-2685G= |