Canonical Allele Identifier:
CA1439212998
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578374C= , CM000666.2:g.12578374C= | GRCh38 |
| NC_000004.11:g.12579998C= , CM000666.1:g.12579998C= | GRCh37 |
| NC_000004.10:g.12189096C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+30968G= | ||
| XR_001741374.1:n.254+44281G= | ||
| XR_925406.3:n.140+30968G= |