Canonical Allele Identifier:
CA2809162095
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237160T>C , CM000679.2:g.30237160T>C | GRCh38 |
| NC_000017.10:g.28564178T>C , CM000679.1:g.28564178T>C | GRCh37 |
| NC_000017.9:g.25588304T>C | NCBI36 |
| NG_011747.2:g.3777A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+90T>C | ||
| XR_001752824.1:n.280+90T>C |