Canonical Allele Identifier:
CA1649534229
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98102413C= , CM000668.2:g.98102413C= | GRCh38 |
| NC_000006.11:g.98550289C= , CM000668.1:g.98550289C= | GRCh37 |
| NC_000006.10:g.98657010C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_245563.2:n.456+3143C= | ||
| XR_942809.1:n.456+3143C= |