Canonical Allele Identifier:
CA1760507851
Gene:
Linked Data
dbSNP Id:
rs913381580
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.5907545G>T , CM000670.2:g.5907545G>T | GRCh38 |
| NC_000008.10:g.5765067G>T , CM000670.1:g.5765067G>T | GRCh37 |
| NC_000008.9:g.5752475G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_941374.1:n.308-7814C>A | ||
| XR_941375.1:n.308-7814C>A | ||
| XR_941376.1:n.406-7814C>A | ||
| XR_941377.1:n.308-7814C>A | ||
| XR_941378.1:n.216-7814C>A | ||
| XR_001745765.1:n.308-7814C>A | ||
| XR_001745766.1:n.406-7814C>A | ||
| XR_001745767.1:n.216-7814C>A | ||
| XR_001745768.1:n.308-7814C>A | ||
| XR_941374.2:n.308-7814C>A | ||
| XR_941375.2:n.308-7814C>A |