Canonical Allele Identifier:
CA1899676337
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.31077342T>G , CM000672.2:g.31077342T>G | GRCh38 |
| NC_000010.10:g.31366271T>G , CM000672.1:g.31366271T>G | GRCh37 |
| NC_000010.9:g.31406277T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001747409.2:n.2299-28597T>G | |
| XR_001747410.2:n.2299-28597T>G | |
| XR_930796.1:n.389-28597T>G | |
| XR_930796.2:n.878-28597T>G |