Canonical Allele Identifier:
CA2570200939
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428070G>A , CM000665.2:g.61428070G>A | GRCh38 |
| NC_000003.11:g.61413744G>A , CM000665.1:g.61413744G>A | GRCh37 |
| NC_000003.10:g.61388784G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-384C>T | ||
| XR_940893.1:n.164+444C>T | ||
| XR_001740725.1:n.202+444C>T | ||
| XR_940892.2:n.203-384C>T |