Canonical Allele Identifier:
CA2544905138
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.8697419A>C , CM000672.2:g.8697419A>C | GRCh38 |
| NC_000010.10:g.8739382A>C , CM000672.1:g.8739382A>C | GRCh37 |
| NC_000010.9:g.8779388A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930641.1:n.33-27618T>G |