Canonical Allele Identifier:
CA682820675
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102497908T>A , CM000674.2:g.102497908T>A | GRCh38 |
| NC_000012.11:g.102891686T>A , CM000674.1:g.102891686T>A | GRCh37 |
| NC_000012.10:g.101415816T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001749289.1:n.1952+14020T>A |