Canonical Allele Identifier:
CA1895268791
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.20610679T= , CM000672.2:g.20610679T= | GRCh38 |
| NC_000010.10:g.20899608T= , CM000672.1:g.20899608T= | GRCh37 |
| NC_000010.9:g.20939614T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930728.1:n.1231T= | ||
| XR_930729.1:n.1276T= | ||
| XR_930730.1:n.1127T= | ||
| XR_930731.1:n.1060T= | ||
| XR_930732.1:n.1082T= | ||
| XR_930733.1:n.1131T= | ||
| XR_001747381.1:n.6079T= | ||
| XR_001747382.1:n.3160T= | ||
| XR_001747383.1:n.5422T= | ||
| XR_001747384.2:n.5273T= | ||
| XR_930729.2:n.2503T= | ||
| XR_930733.2:n.5377T= |