Canonical Allele Identifier:
CA1704517798
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.46033000C= , CM000669.2:g.46033000C= | GRCh38 |
| NC_000007.13:g.46072598C= , CM000669.1:g.46072598C= | GRCh37 |
| NC_000007.12:g.46039123C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745203.1:n.1270-3618C= |