Canonical Allele Identifier:
CA1697889656
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897373G= , CM000669.2:g.30897373G= | GRCh38 |
| NC_000007.13:g.30936988G= , CM000669.1:g.30936988G= | GRCh37 |
| NC_000007.12:g.30903513G= | NCBI36 |
| NG_007475.2:g.48980G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000509504.2:c.621+14380G= |