Canonical Allele Identifier:
CA16139842
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.34921177T>C , CM000665.2:g.34921177T>C | GRCh38 |
| NC_000003.11:g.34962669T>C , CM000665.1:g.34962669T>C | GRCh37 |
| NC_000003.10:g.34937673T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110817.1:n.207-41711A>G |