Canonical Allele Identifier:
CA1941455894
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122458274T= , CM000672.2:g.122458274T= | GRCh38 |
| NC_000010.10:g.124217790T= , CM000672.1:g.124217790T= | GRCh37 |
| NC_000010.9:g.124207780T= | NCBI36 |
| NG_011554.1:g.1750T= | |
| NG_011725.1:g.8612T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946382.1:n.1827+221A= | ||
| XR_946383.1:n.1827+221A= | ||
| XR_946384.1:n.1576+221A= | ||
| XR_946385.1:n.1827+221A= | ||
| XR_946382.2:n.1855+221A= | ||
| XR_946383.2:n.1855+221A= | ||
| XR_946384.2:n.1580+221A= | ||
| XR_946385.2:n.1855+221A= |