Linked Data
dbSNP Id:
rs9404941
gnomAD v2:
6-31622816-T-C
gnomAD v3:
6-31655039-T-C
gnomAD v4:
6-31655039-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31655039T>C , CM000668.2:g.31655039T>C | GRCh38 |
| NC_000006.11:g.31622816T>C , CM000668.1:g.31622816T>C | GRCh37 |
| NC_000006.10:g.31730795T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375918.6:c.-102-1433T>C (APOM) | ENSP00000365083.2:n.-102-1433T>C | |
| ENST00000375920.8:c.-102-1433T>C (APOM) | ENSP00000365085.4:n.-102-1433T>C | |
| NM_001256169.1:c.-102-1433T>C (APOM) | NP_001243098.1:n.-102-1433T>C | |
| NR_045828.1:n.143-1433T>C (APOM) | ||
| XM_011514895.1:c.-13-3263A>G (BAG6) | XP_011513197.1:n.-13-3263A>G | |
| XM_017011279.2:c.-13-3263A>G (BAG6) | XP_016866768.1:n.-13-3263A>G | |
| XM_024446545.1:c.-14+2725A>G (BAG6) | XP_024302313.1:n.-14+2725A>G | |
| NM_001256169.2:c.-102-1433T>C (APOM) | NP_001243098.1:n.-102-1433T>C | |
| NR_045828.2:n.149-1433T>C (APOM) |