Canonical Allele Identifier:
CA1653130372
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.105805124T= , CM000668.2:g.105805124T= | GRCh38 |
| NC_000006.11:g.106252999T= , CM000668.1:g.106252999T= | GRCh37 |
| NC_000006.10:g.106359692T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_942835.1:n.510+24933A= | ||
| XR_001744274.1:n.438+24933A= | ||
| XR_001744275.1:n.337+24933A= |