Canonical Allele Identifier:
CA1139933659
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.90478350A= , CM000663.2:g.90478350A= | GRCh38 |
| NC_000001.10:g.90943907A= , CM000663.1:g.90943907A= | GRCh37 |
| NC_000001.9:g.90716495A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947591.1:n.139+418T= | ||
| XR_947591.2:n.151+418T= |