Canonical Allele Identifier:
CA1674885890
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812652C= , CM000668.2:g.155812652C= | GRCh38 |
| NC_000006.11:g.156133786C= , CM000668.1:g.156133786C= | GRCh37 |
| NC_000006.10:g.156175478C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19233C= | ||
| XR_943146.1:n.645-613G= | ||
| XR_001744423.1:n.699-613G= | ||
| XR_001744424.1:n.79+19233C= |