Canonical Allele Identifier:
CA780105996
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.49640844T>G , CM000680.2:g.49640844T>G | GRCh38 |
| NC_000018.9:g.47167214T>G , CM000680.1:g.47167214T>G | GRCh37 |
| NC_000018.8:g.45421212T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935461.1:n.162-21190T>G | ||
| XR_001753446.1:n.898-21190T>G |