Canonical Allele Identifier:
CA1960019971
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.27484076G= , CM000673.2:g.27484076G= | GRCh38 |
| NC_000011.9:g.27505623G= , CM000673.1:g.27505623G= | GRCh37 |
| NC_000011.8:g.27462199G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496450.1:n.227G= |