Canonical Allele Identifier:
CA2293960131
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31756629T= , CM000680.2:g.31756629T= | GRCh38 |
| NC_000018.9:g.29336592T= , CM000680.1:g.29336592T= | GRCh37 |
| NC_000018.8:g.27590590T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935338.1:n.66-5510T= |