Canonical Allele Identifier:
CA1496041089
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.134616564T= , CM000666.2:g.134616564T= | GRCh38 |
| NC_000004.11:g.135537719T= , CM000666.1:g.135537719T= | GRCh37 |
| NC_000004.10:g.135757169T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939212.1:n.411-23016T= | ||
| XR_939214.1:n.393-23016T= | ||
| XR_939214.2:n.393-23016T= |