Canonical Allele Identifier:
CA2129379026
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36384775C= , CM000676.2:g.36384775C= | GRCh38 |
| NC_000014.8:g.36853980C= , CM000676.1:g.36853980C= | GRCh37 |
| NC_000014.7:g.35923731C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12384C= | XP_011535730.1:n.319-12384C= | |
| XR_943756.1:n.358+23679C= |