Canonical Allele Identifier:
CA14913498
Community Standard Title: NC_000021.9:g.42358786A>G
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.42358786A>G , CM000683.2:g.42358786A>G | GRCh38 |
| NC_000021.8:g.43778895A>G , CM000683.1:g.43778895A>G | GRCh37 |
| NC_000021.7:g.42651964A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001755064.1:n.2096A>G | |
| XR_001755065.1:n.1954A>G | |
| XR_001755066.1:n.2096A>G | |
| XR_001755067.1:n.1388A>G | |
| XR_937750.1:n.2092A>G | |
| XR_937750.2:n.2096A>G | |
| XR_937751.1:n.2092A>G | |
| XR_937752.1:n.1950A>G | |
| XR_937753.1:n.1384A>G | |
| XR_937754.1:n.2092A>G | |
| XR_937754.2:n.2096A>G | |
| XR_937755.1:n.2092A>G | |
| XR_937755.2:n.2096A>G |