Canonical Allele Identifier:
CA1480021950
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99474283T= , CM000666.2:g.99474283T= | GRCh38 |
| NC_000004.11:g.100395440T= , CM000666.1:g.100395440T= | GRCh37 |
| NC_000004.10:g.100614463T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506494.1:n.243-2421A= |