Canonical Allele Identifier:
CA1991735980
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.92917836C= , CM000673.2:g.92917836C= | GRCh38 |
| NC_000011.9:g.92651002C= , CM000673.1:g.92651002C= | GRCh37 |
| NC_000011.8:g.92290650C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634657.1:n.81+1872C= |