Canonical Allele Identifier:
CA1697889659
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30897382A= , CM000669.2:g.30897382A= | GRCh38 |
| NC_000007.13:g.30936997A= , CM000669.1:g.30936997A= | GRCh37 |
| NC_000007.12:g.30903522A= | NCBI36 |
| NG_007475.2:g.48989A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000509504.2:c.621+14389A= |