Canonical Allele Identifier:
CA1937625692
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114021768T= , CM000672.2:g.114021768T= | GRCh38 |
| NC_000010.10:g.115781527T= , CM000672.1:g.115781527T= | GRCh37 |
| NC_000010.9:g.115771517T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946331.1:n.438-737T= | ||
| XR_946332.1:n.306-737T= |