Canonical Allele Identifier:
CA16273898
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.97571204A>G , CM000668.2:g.97571204A>G | GRCh38 |
| NC_000006.11:g.98019080A>G , CM000668.1:g.98019080A>G | GRCh37 |
| NC_000006.10:g.98125801A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110757.1:n.512-40964A>G |