Canonical Allele Identifier:
CA1697903925
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.30911505G= , CM000669.2:g.30911505G= | GRCh38 |
| NC_000007.13:g.30951120G= , CM000669.1:g.30951120G= | GRCh37 |
| NC_000007.12:g.30917645G= | NCBI36 |
| NG_007475.2:g.63112G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000509504.2:c.622-488G= |