Canonical Allele Identifier:
CA1369169835
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61428049C= , CM000665.2:g.61428049C= | GRCh38 |
| NC_000003.11:g.61413723C= , CM000665.1:g.61413723C= | GRCh37 |
| NC_000003.10:g.61388763C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_940892.1:n.165-363G= | ||
| XR_940893.1:n.164+465G= | ||
| XR_001740725.1:n.202+465G= | ||
| XR_940892.2:n.203-363G= |