Canonical Allele Identifier:
CA1734069030
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.110407907C= , CM000669.2:g.110407907C= | GRCh38 |
| NC_000007.13:g.110047964C= , CM000669.1:g.110047964C= | GRCh37 |
| NC_000007.12:g.109835200C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001744982.1:n.604+24904G= | ||
| XR_927863.2:n.367+24904G= |