Canonical Allele Identifier:
CA1630779431
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.57982677G= , CM000668.2:g.57982677G= | GRCh38 |
| NC_000006.11:g.58308955G= , CM000668.1:g.58308955G= | GRCh37 |
| NC_000006.10:g.58416914G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926906.1:n.321+11021G= | ||
| XR_001744180.1:n.3471+11021G= | ||
| XR_001744183.1:n.3471+11021G= | ||
| XR_001744184.1:n.3471+11021G= | ||
| XR_001744185.1:n.3471+11021G= |