Canonical Allele Identifier:
CA1439212558
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.12577929G= , CM000666.2:g.12577929G= | GRCh38 |
| NC_000004.11:g.12579553G= , CM000666.1:g.12579553G= | GRCh37 |
| NC_000004.10:g.12188651G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925406.1:n.106+31413C= | ||
| XR_001741374.1:n.254+44726C= | ||
| XR_925406.3:n.140+31413C= |