Canonical Allele Identifier:
CA1142578080
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800676C= , CM000663.2:g.192800676C= | GRCh38 |
| NC_000001.10:g.192769806C= , CM000663.1:g.192769806C= | GRCh37 |
| NC_000001.9:g.191036429C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.106C= |