Canonical Allele Identifier:
CA14888672
Community Standard Title: NC_000021.9:g.15440893T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.15440893T>C , CM000683.2:g.15440893T>C | GRCh38 |
| NC_000021.8:g.16813212T>C , CM000683.1:g.16813212T>C | GRCh37 |
| NC_000021.7:g.15735083T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001754965.2:n.468+3131A>G | |
| XR_001754970.2:n.468+3131A>G | |
| XR_001754971.2:n.468+3131A>G | |
| XR_937593.1:n.552+333A>G |