Canonical Allele Identifier:
CA2170931659
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38614870A= , CM000677.2:g.38614870A= | GRCh38 |
| NC_000015.9:g.38907071A= , CM000677.1:g.38907071A= | GRCh37 |
| NC_000015.8:g.36694363A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001751736.1:n.281+2415A= |