Canonical Allele Identifier:
CA1267947480
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016274C= , CM000664.2:g.88016274C= | GRCh38 |
| NC_000002.11:g.88315793C= , CM000664.1:g.88315793C= | GRCh37 |
| NC_000002.10:g.88096908C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.619C= | ||
| XR_940336.3:n.619C= |