Canonical Allele Identifier:
CA1967478799
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.43214511A= , CM000673.2:g.43214511A= | GRCh38 |
| NC_000011.9:g.43236061A= , CM000673.1:g.43236061A= | GRCh37 |
| NC_000011.8:g.43192637A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000533565.1:n.129+54754T= |