Canonical Allele Identifier:
CA1557963452
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79550012T= , CM000667.2:g.79550012T= | GRCh38 |
| NC_000005.9:g.78845835T= , CM000667.1:g.78845835T= | GRCh37 |
| NC_000005.8:g.78881591T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948497.1:n.72+2368T= | ||
| XR_948498.1:n.159+2175T= | ||
| XR_948499.1:n.67+1710T= | ||
| XR_948497.2:n.72+2368T= | ||
| XR_948498.2:n.159+2175T= | ||
| XR_948499.2:n.225+1710T= |