Canonical Allele Identifier:
CA2686840879
Gene:
Linked Data
gnomAD v4:
8-31176558-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.31176558G>T , CM000670.2:g.31176558G>T | GRCh38 |
| NC_000008.10:g.31034074G>T , CM000670.1:g.31034074G>T | GRCh37 |
| NC_000008.9:g.31153616G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_949642.1:n.239G>T | ||
| XR_949643.1:n.87+134C>A | ||
| XR_949644.1:n.87+134C>A | ||
| XR_949645.1:n.87+134C>A | ||
| XR_949646.1:n.87+134C>A | ||
| XR_949647.1:n.700+134C>A | ||
| XR_949648.1:n.602+134C>A |