Canonical Allele Identifier:
CA735211418
Gene:
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34285335T>A , CM000663.2:g.34285335T>A | GRCh38 |
| NC_000001.10:g.34750936T>A , CM000663.1:g.34750936T>A | GRCh37 |
| NC_000001.9:g.34523523T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947169.1:n.493+4328T>A | ||
| XR_947169.2:n.493+4328T>A |