Canonical Allele Identifier:
CA1318169453
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.195007038T= , CM000664.2:g.195007038T= | GRCh38 |
| NC_000002.11:g.195871762T= , CM000664.1:g.195871762T= | GRCh37 |
| NC_000002.10:g.195580007T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001739836.1:n.553+52397A= |