Canonical Allele Identifier:
CA1620959068
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35569629T= , CM000668.2:g.35569629T= | GRCh38 |
| NC_000006.11:g.35537406T= , CM000668.1:g.35537406T= | GRCh37 |
| NC_000006.10:g.35645384T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_242006.2:n.433-23401T= | ||
| XR_242006.3:n.462-23401T= |