Canonical Allele Identifier:
CA185510393
Gene:
Linked Data
dbSNP Id:
rs928507267
gnomAD v3:
8-125474152-G-A
gnomAD v4:
8-125474152-G-A
MyVariant Identifiers:
chr8:g.125474152G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.125474152G>A , CM000670.2:g.125474152G>A | GRCh38 |
| NC_000008.10:g.126486394G>A , CM000670.1:g.126486394G>A | GRCh37 |
| NC_000008.9:g.126555576G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928628.1:n.256+838G>A |