Canonical Allele Identifier:
CA1605276813
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465839C= , CM000668.2:g.465839C= | GRCh38 |
| NC_000006.11:g.465839C= , CM000668.1:g.465839C= | GRCh37 |
| NC_000006.10:g.410839C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926364.1:n.2714+12114C= | ||
| XR_926365.1:n.2548+12114C= | ||
| XR_001743914.1:n.482-9369C= |