Canonical Allele Identifier:
CA1502599078
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.148649464T= , CM000666.2:g.148649464T= | GRCh38 |
| NC_000004.11:g.149570616T= , CM000666.1:g.149570616T= | GRCh37 |
| NC_000004.10:g.149790066T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939336.1:n.437-30596A= | ||
| XR_001741441.1:n.1745+104880T= | ||
| XR_939336.3:n.2921-30596A= |