Canonical Allele Identifier:
CA1591798642
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.152354361T= , CM000667.2:g.152354361T= | GRCh38 |
| NC_000005.9:g.151733922T= , CM000667.1:g.151733922T= | GRCh37 |
| NC_000005.8:g.151714115T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_944433.1:n.196+16498T= | ||
| XR_944433.2:n.197+16498T= |