Canonical Allele Identifier:
CA2390766332
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.42358786A>T , CM000683.2:g.42358786A>T | GRCh38 |
| NC_000021.8:g.43778895A>T , CM000683.1:g.43778895A>T | GRCh37 |
| NC_000021.7:g.42651964A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_937750.1:n.2092A>T | ||
| XR_937751.1:n.2092A>T | ||
| XR_937752.1:n.1950A>T | ||
| XR_937753.1:n.1384A>T | ||
| XR_937754.1:n.2092A>T | ||
| XR_937755.1:n.2092A>T | ||
| XR_001755064.1:n.2096A>T | ||
| XR_001755065.1:n.1954A>T | ||
| XR_001755066.1:n.2096A>T | ||
| XR_001755067.1:n.1388A>T | ||
| XR_937750.2:n.2096A>T | ||
| XR_937754.2:n.2096A>T | ||
| XR_937755.2:n.2096A>T |