Canonical Allele Identifier:
CA2378344930
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.15440851T= , CM000683.2:g.15440851T= | GRCh38 |
| NC_000021.8:g.16813170T= , CM000683.1:g.16813170T= | GRCh37 |
| NC_000021.7:g.15735041T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_937593.1:n.552+375A= | ||
| XR_001754965.2:n.468+3173A= | ||
| XR_001754970.2:n.468+3173A= | ||
| XR_001754971.2:n.468+3173A= |