Canonical Allele Identifier:
CA2320960038
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7522601C= , CM000681.2:g.7522601C= | GRCh38 |
| NC_000019.9:g.7587487C= , CM000681.1:g.7587487C= | GRCh37 |
| NC_000019.8:g.7493487C= | NCBI36 |
| NG_015806.1:g.4992C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936293.1:n.926+241G= | ||
| XR_936294.1:n.926+241G= | ||
| XR_936295.1:n.570+241G= | ||
| XR_936293.2:n.952+241G= | ||
| XR_936294.2:n.952+241G= |