Linked Data
dbSNP Id:
rs987594596
gnomAD v2:
6-31621825-C-G
gnomAD v3:
6-31654048-C-G
gnomAD v4:
6-31654048-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31654048C>G , CM000668.2:g.31654048C>G | GRCh38 |
| NC_000006.11:g.31621825C>G , CM000668.1:g.31621825C>G | GRCh37 |
| NC_000006.10:g.31729804C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375918.6:c.-103+1497C>G (APOM) | ENSP00000365083.2:n.-103+1497C>G | |
| ENST00000375920.8:c.-103+1497C>G (APOM) | ENSP00000365085.4:n.-103+1497C>G | |
| NM_001256169.1:c.-103+1497C>G (APOM) | NP_001243098.1:n.-103+1497C>G | |
| NR_045828.1:n.142+1497C>G (APOM) | ||
| XM_011514895.1:c.-13-2272G>C (BAG6) | XP_011513197.1:n.-13-2272G>C | |
| XM_017011279.2:c.-13-2272G>C (BAG6) | XP_016866768.1:n.-13-2272G>C | |
| XM_024446545.1:c.-13-2272G>C (BAG6) | XP_024302313.1:n.-13-2272G>C | |
| NM_001256169.2:c.-103+1497C>G (APOM) | NP_001243098.1:n.-103+1497C>G | |
| NR_045828.2:n.148+1497C>G (APOM) |