Canonical Allele Identifier:
CA1595159035
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159580683T= , CM000667.2:g.159580683T= | GRCh38 |
| NC_000005.9:g.159007691T= , CM000667.1:g.159007691T= | GRCh37 |
| NC_000005.8:g.158940269T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_941139.1:n.2075+248T= | ||
| XR_941140.1:n.2075+248T= | ||
| XR_941141.1:n.570+248T= | ||
| XR_941139.2:n.2229+248T= |