Canonical Allele Identifier:
CA2056175897
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.95318100A>G , CM000674.2:g.95318100A>G | GRCh38 |
| NC_000012.11:g.95711876A>G , CM000674.1:g.95711876A>G | GRCh37 |
| NC_000012.10:g.94236007A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636165.1:n.1059-6646T>C |