Canonical Allele Identifier:
CA1639634900
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.77465335G= , CM000668.2:g.77465335G= | GRCh38 |
| NC_000006.11:g.78175052G= , CM000668.1:g.78175052G= | GRCh37 |
| NC_000006.10:g.78231771G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_942706.1:n.545-9191G= | ||
| XR_942707.1:n.545-9191G= | ||
| XR_942708.1:n.545-9191G= | ||
| XR_942709.1:n.545-9191G= | ||
| XR_942708.2:n.545-9191G= |