Canonical Allele Identifier:
CA2332763267
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521962T= , CM000681.2:g.33521962T= | GRCh38 |
| NC_000019.9:g.34012868T= , CM000681.1:g.34012868T= | GRCh37 |
| NC_000019.8:g.38704708T= | NCBI36 |
| NG_013358.1:g.4932A= | |
| NG_013358.2:g.4932A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.21T= | ||
| XR_935919.1:n.16T= | ||
| XR_001754035.2:n.29T= | ||
| XR_935918.2:n.29T= |