Canonical Allele Identifier:
CA1320446152
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.200033192C= , CM000664.2:g.200033192C= | GRCh38 |
| NC_000002.11:g.200897915C= , CM000664.1:g.200897915C= | GRCh37 |
| NC_000002.10:g.200606160C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923778.1:n.178-22296G= |