Canonical Allele Identifier:
CA1620197396
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33857581G= , CM000668.2:g.33857581G= | GRCh38 |
| NC_000006.11:g.33825358G= , CM000668.1:g.33825358G= | GRCh37 |
| NC_000006.10:g.33933336G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926720.1:n.237+1143G= | ||
| XR_926721.1:n.237+1143G= | ||
| XR_926722.1:n.237+1143G= | ||
| XR_926723.1:n.235+1143G= | ||
| XR_926724.1:n.237+1143G= | ||
| XR_926725.1:n.236+1143G= | ||
| XR_926720.2:n.237+1143G= |