Canonical Allele Identifier:
CA1369169847
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428073C= , CM000665.2:g.61428073C= | GRCh38 |
| NC_000003.11:g.61413747C= , CM000665.1:g.61413747C= | GRCh37 |
| NC_000003.10:g.61388787C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-387G= | ||
| XR_940893.1:n.164+441G= | ||
| XR_001740725.1:n.202+441G= | ||
| XR_940892.2:n.203-387G= |