Canonical Allele Identifier:
CA2031042685
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.40373549A= , CM000674.2:g.40373549A= | GRCh38 |
| NC_000012.11:g.40767351A= , CM000674.1:g.40767351A= | GRCh37 |
| NC_000012.10:g.39053618A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_944868.1:n.485-18722T= | ||
| XR_944869.1:n.485-1497T= | ||
| XR_001749087.1:n.380-1497T= | ||
| XR_001749088.1:n.347-1497T= | ||
| XR_944868.2:n.485-18722T= | ||
| XR_944869.2:n.485-1497T= |