Canonical Allele Identifier:
CA2809162145
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237266A>C , CM000679.2:g.30237266A>C | GRCh38 |
| NC_000017.10:g.28564284A>C , CM000679.1:g.28564284A>C | GRCh37 |
| NC_000017.9:g.25588410A>C | NCBI36 |
| NG_011747.2:g.3671T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+196A>C | ||
| XR_001752824.1:n.280+196A>C |