Canonical Allele Identifier:
CA1245488683
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.37817201C= , CM000664.2:g.37817201C= | GRCh38 |
| NC_000002.11:g.38044344C= , CM000664.1:g.38044344C= | GRCh37 |
| NC_000002.10:g.37897848C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456500.1:n.287C= |