Canonical Allele Identifier:
CA309276912
Gene:
MyVariant.info:
GRCh38
chr19:g.44466713G>T
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.40648096 (SAS)
Genomes Max Group AF
0.40648096 (SAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44466713G>T , CM000681.2:g.44466713G>T | GRCh38 |