Canonical Allele Identifier:
CA1369169812
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.61427995A= , CM000665.2:g.61427995A= | GRCh38 |
| NC_000003.11:g.61413669A= , CM000665.1:g.61413669A= | GRCh37 |
| NC_000003.10:g.61388709A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940892.1:n.165-309T= | ||
| XR_940893.1:n.164+519T= | ||
| XR_001740725.1:n.202+519T= | ||
| XR_940892.2:n.203-309T= |