Canonical Allele Identifier:
CA892352029
Gene:
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.68343640G>A , CM000664.2:g.68343640G>A | GRCh38 |
| NC_000002.11:g.68570772G>A , CM000664.1:g.68570772G>A | GRCh37 |
| NC_000002.10:g.68424276G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_427045.2:n.4651+853G>A | ||
| XR_940224.1:n.292+853G>A | ||
| XR_940224.3:n.328+853G>A |