Canonical Allele Identifier:
CA1139830658
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34285335T= , CM000663.2:g.34285335T= | GRCh38 |
| NC_000001.10:g.34750936T= , CM000663.1:g.34750936T= | GRCh37 |
| NC_000001.9:g.34523523T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947169.1:n.493+4328T= | ||
| XR_947169.2:n.493+4328T= |