Canonical Allele Identifier:
CA1677169884
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668477C= , CM000668.2:g.160668477C= | GRCh38 |
| NC_000006.11:g.161089509C= , CM000668.1:g.161089509C= | GRCh37 |
| NC_000006.10:g.161009499C= | NCBI36 |
| NG_016147.1:g.2899G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2104G= |