Canonical Allele Identifier:
CA1704517764
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.46032935C= , CM000669.2:g.46032935C= | GRCh38 |
| NC_000007.13:g.46072533C= , CM000669.1:g.46072533C= | GRCh37 |
| NC_000007.12:g.46039058C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745203.1:n.1270-3683C= |