Canonical Allele Identifier:
CA1140297177
Community Standard Title: NC_000001.11:g.116495665T=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.116495665T= , CM000663.2:g.116495665T= | GRCh38 |
| NC_000001.10:g.117038287T= , CM000663.1:g.117038287T= | GRCh37 |
| NC_000001.9:g.116839810T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_002958352.1:n.8802+2172T= | |
| XR_947732.1:n.8955A= | |
| XR_947733.1:n.8866A= | |
| XR_947734.1:n.3635A= | |
| XR_947735.1:n.6355-1610T= | |
| XR_947736.1:n.4037-1610T= |