Canonical Allele Identifier:
CA1369169842
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428061A= , CM000665.2:g.61428061A= | GRCh38 |
| NC_000003.11:g.61413735A= , CM000665.1:g.61413735A= | GRCh37 |
| NC_000003.10:g.61388775A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-375T= | ||
| XR_940893.1:n.164+453T= | ||
| XR_001740725.1:n.202+453T= | ||
| XR_940892.2:n.203-375T= |