Canonical Allele Identifier:
CA16385523
Gene:
gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.31090176C>T , CM000672.2:g.31090176C>T | GRCh38 |
| NC_000010.10:g.31379105C>T , CM000672.1:g.31379105C>T | GRCh37 |
| NC_000010.9:g.31419111C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930796.1:n.389-15763C>T | ||
| XR_001747409.2:n.2299-15763C>T | ||
| XR_001747410.2:n.2299-15763C>T | ||
| XR_930796.2:n.878-15763C>T |