Canonical Allele Identifier:
CA1267947489
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016283T= , CM000664.2:g.88016283T= | GRCh38 |
| NC_000002.11:g.88315802T= , CM000664.1:g.88315802T= | GRCh37 |
| NC_000002.10:g.88096917T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.628T= | ||
| XR_940336.3:n.628T= |