Canonical Allele Identifier:
CA1611926813
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.14636732T= , CM000668.2:g.14636732T= | GRCh38 |
| NC_000006.11:g.14636963T= , CM000668.1:g.14636963T= | GRCh37 |
| NC_000006.10:g.14744942T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241980.2:n.173+7219A= | ||
| XR_926515.1:n.173+7219A= | ||
| XR_926517.1:n.84+5430A= | ||
| XR_001743992.1:n.559+5430A= | ||
| XR_241980.3:n.421+7219A= |