Canonical Allele Identifier:
CA1906417796
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44390758C= , CM000672.2:g.44390758C= | GRCh38 |
| NC_000010.10:g.44886206C= , CM000672.1:g.44886206C= | GRCh37 |
| NC_000010.9:g.44206212C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001747298.1:n.67+926C= |