Canonical Allele Identifier:
CA2055289532
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.93293233C= , CM000674.2:g.93293233C= | GRCh38 |
| NC_000012.11:g.93687009C= , CM000674.1:g.93687009C= | GRCh37 |
| NC_000012.10:g.92211140C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040096.1:n.329+34794G= |