Canonical Allele Identifier:
CA885975089
Community Standard Title: NC_000001.11:g.116495665T>A
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.116495665T>A , CM000663.2:g.116495665T>A | GRCh38 |
| NC_000001.10:g.117038287T>A , CM000663.1:g.117038287T>A | GRCh37 |
| NC_000001.9:g.116839810T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_002958352.1:n.8802+2172T>A | |
| XR_947732.1:n.8955A>T | |
| XR_947733.1:n.8866A>T | |
| XR_947734.1:n.3635A>T | |
| XR_947735.1:n.6355-1610T>A | |
| XR_947736.1:n.4037-1610T>A |