Canonical Allele Identifier:
CA1889344487
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.8697500C= , CM000672.2:g.8697500C= | GRCh38 |
| NC_000010.10:g.8739463C= , CM000672.1:g.8739463C= | GRCh37 |
| NC_000010.9:g.8779469C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930641.1:n.33-27699G= |