Canonical Allele Identifier:
CA2284239348
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.10321256C= , CM000680.2:g.10321256C= | GRCh38 |
| NC_000018.9:g.10321253C= , CM000680.1:g.10321253C= | GRCh37 |
| NC_000018.8:g.10311253C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935138.1:n.665+892G= | ||
| XR_001753344.1:n.650+892G= | ||
| XR_001753345.1:n.865G= | ||
| XR_001753346.1:n.549+892G= |