Canonical Allele Identifier:
CA1674890211
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155817575T= , CM000668.2:g.155817575T= | GRCh38 |
| NC_000006.11:g.156138709T= , CM000668.1:g.156138709T= | GRCh37 |
| NC_000006.10:g.156180401T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+24156T= | ||
| XR_943146.1:n.552-2905A= | ||
| XR_001744423.1:n.606-2905A= | ||
| XR_001744424.1:n.79+24156T= |