Canonical Allele Identifier:
CA2504463671
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237132T>G , CM000679.2:g.30237132T>G | GRCh38 |
| NC_000017.10:g.28564150T>G , CM000679.1:g.28564150T>G | GRCh37 |
| NC_000017.9:g.25588276T>G | NCBI36 |
| NG_011747.2:g.3805A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+62T>G | ||
| XR_001752824.1:n.280+62T>G |