Canonical Allele Identifier:
CA1890759229
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.11678309A= , CM000672.2:g.11678309A= | GRCh38 |
| NC_000010.10:g.11720308A= , CM000672.1:g.11720308A= | GRCh37 |
| NC_000010.9:g.11760314A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_002957063.1:n.932-950A= | |
| XR_930659.1:n.40-950A= | |
| XR_930660.1:n.466-950A= | |
| XR_930661.1:n.784-950A= | |
| XR_930661.2:n.785-950A= | |
| XR_930662.1:n.2156+1565T= | |
| XR_930662.3:n.2156+1565T= |