Canonical Allele Identifier:
CA170431762
Gene:
MyVariant.info:
GRCh38
chr8:g.2021565G>T
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.43052022 (AFR)
Genomes Max Group AF
0.43052022 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.2021565G>T , CM000670.2:g.2021565G>T | GRCh38 |