Canonical Allele Identifier:
CA1677169862
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668422T= , CM000668.2:g.160668422T= | GRCh38 |
| NC_000006.11:g.161089454T= , CM000668.1:g.161089454T= | GRCh37 |
| NC_000006.10:g.161009444T= | NCBI36 |
| NG_016147.1:g.2954A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2049A= |