MyVariant.info:
GRCh38
chr14:g.22530666G>T
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.89501739 (AFR)
Genomes Max Group AF
0.89501739 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.22530666G>T , CM000676.2:g.22530666G>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000616778.4:c.65-16840G>T | ENSP00000482550.1:n.65-16840G>T |