Canonical Allele Identifier:
CA1439212863
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12578235C= , CM000666.2:g.12578235C= | GRCh38 |
| NC_000004.11:g.12579859C= , CM000666.1:g.12579859C= | GRCh37 |
| NC_000004.10:g.12188957C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_925406.1:n.106+31107G= | ||
| XR_001741374.1:n.254+44420G= | ||
| XR_925406.3:n.140+31107G= |