Canonical Allele Identifier:
CA838948322
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.45968511G>T , CM000669.2:g.45968511G>T | GRCh38 |
| NC_000007.13:g.46008110G>T , CM000669.1:g.46008110G>T | GRCh37 |
| NC_000007.12:g.45974635G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927237.1:n.322-9008G>T | ||
| XR_927238.1:n.322-9008G>T | ||
| XR_927239.1:n.322-9008G>T | ||
| XR_927240.1:n.322-9008G>T | ||
| XR_001745202.1:n.327-9008G>T | ||
| XR_001745203.1:n.327-9008G>T |