Canonical Allele Identifier:
CA1674885611
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812395C= , CM000668.2:g.155812395C= | GRCh38 |
| NC_000006.11:g.156133529C= , CM000668.1:g.156133529C= | GRCh37 |
| NC_000006.10:g.156175221C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+18976C= | ||
| XR_943146.1:n.645-356G= | ||
| XR_001744423.1:n.699-356G= | ||
| XR_001744424.1:n.79+18976C= |