Canonical Allele Identifier:
CA1482549867
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.104923116T= , CM000666.2:g.104923116T= | GRCh38 |
| NC_000004.11:g.105844273T= , CM000666.1:g.105844273T= | GRCh37 |
| NC_000004.10:g.106063722T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939034.1:n.79-495T= | ||
| XR_939035.1:n.79-495T= |