Canonical Allele Identifier:
CA2112050559
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.94853033C= , CM000675.2:g.94853033C= | GRCh38 |
| NC_000013.10:g.95505287C= , CM000675.1:g.95505287C= | GRCh37 |
| NC_000013.9:g.94303288C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110754.1:n.257-52431C= |