Canonical Allele Identifier:
CA15980111
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.52408842A>G , CM000682.2:g.52408842A>G | GRCh38 |
| NC_000020.10:g.51025381A>G , CM000682.1:g.51025381A>G | GRCh37 |
| NC_000020.9:g.50458788A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001754670.1:n.434+68190A>G | ||
| XR_001754671.1:n.434+68190A>G | ||
| XR_002958559.1:n.471+68190A>G |