Canonical Allele Identifier:
CA2112050656
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.94853076A= , CM000675.2:g.94853076A= | GRCh38 |
| NC_000013.10:g.95505330A= , CM000675.1:g.95505330A= | GRCh37 |
| NC_000013.9:g.94303331A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110754.1:n.257-52388A= |