Canonical Allele Identifier:
CA1704484915
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.45968511G= , CM000669.2:g.45968511G= | GRCh38 |
| NC_000007.13:g.46008110G= , CM000669.1:g.46008110G= | GRCh37 |
| NC_000007.12:g.45974635G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927237.1:n.322-9008G= | ||
| XR_927238.1:n.322-9008G= | ||
| XR_927239.1:n.322-9008G= | ||
| XR_927240.1:n.322-9008G= | ||
| XR_001745202.1:n.327-9008G= | ||
| XR_001745203.1:n.327-9008G= |