Canonical Allele Identifier:
CA1608913943
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.8169732T= , CM000668.2:g.8169732T= | GRCh38 |
| NC_000006.11:g.8169965T= , CM000668.1:g.8169965T= | GRCh37 |
| NC_000006.10:g.8114964T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926440.1:n.82+11472T= | ||
| XR_926441.1:n.189+1812T= | ||
| XR_926442.1:n.82+11472T= | ||
| XR_926443.1:n.82+11472T= | ||
| XR_001743950.1:n.179+1812T= | ||
| XR_926440.2:n.74+11472T= | ||
| XR_926441.2:n.179+1812T= | ||
| XR_926443.2:n.83+11472T= |