Canonical Allele Identifier:
CA1677169890
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668489C= , CM000668.2:g.160668489C= | GRCh38 |
| NC_000006.11:g.161089521C= , CM000668.1:g.161089521C= | GRCh37 |
| NC_000006.10:g.161009511C= | NCBI36 |
| NG_016147.1:g.2887G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2116G= |