Canonical Allele Identifier:
CA1468682181
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.74554117T= , CM000666.2:g.74554117T= | GRCh38 |
| NC_000004.11:g.75419834T= , CM000666.1:g.75419834T= | GRCh37 |
| NC_000004.10:g.75638698T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741513.1:n.167-1285A= |