Canonical Allele Identifier:
CA1439212598
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12577983A= , CM000666.2:g.12577983A= | GRCh38 |
| NC_000004.11:g.12579607A= , CM000666.1:g.12579607A= | GRCh37 |
| NC_000004.10:g.12188705A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31359T= | ||
| XR_001741374.1:n.254+44672T= | ||
| XR_925406.3:n.140+31359T= |