gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00012872 (AMR)
Genomes Max Group AF
0.00012872 (AMR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31654885A>G , CM000668.2:g.31654885A>G | GRCh38 |
| NC_000006.11:g.31622662A>G , CM000668.1:g.31622662A>G | GRCh37 |
| NC_000006.10:g.31730641A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375918.6:c.-102-1587A>G (APOM) | ENSP00000365083.2:n.-102-1587A>G | |
| ENST00000375920.8:c.-102-1587A>G (APOM) | ENSP00000365085.4:n.-102-1587A>G | |
| NM_001256169.1:c.-102-1587A>G (APOM) | NP_001243098.1:n.-102-1587A>G | |
| NR_045828.1:n.143-1587A>G (APOM) | ||
| XM_011514895.1:c.-13-3109T>C (BAG6) | XP_011513197.1:n.-13-3109T>C | |
| XM_017011279.2:c.-13-3109T>C (BAG6) | XP_016866768.1:n.-13-3109T>C | |
| XM_024446545.1:c.-14+2879T>C (BAG6) | XP_024302313.1:n.-14+2879T>C | |
| NM_001256169.2:c.-102-1587A>G (APOM) | NP_001243098.1:n.-102-1587A>G | |
| NR_045828.2:n.149-1587A>G (APOM) |