Linked Data
dbSNP Id:
rs9267528
gnomAD v2:
6-31622141-C-T
gnomAD v3:
6-31654364-C-T
gnomAD v4:
6-31654364-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31654364C>T , CM000668.2:g.31654364C>T | GRCh38 |
| NC_000006.11:g.31622141C>T , CM000668.1:g.31622141C>T | GRCh37 |
| NC_000006.10:g.31730120C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375918.6:c.-103+1813C>T (APOM) | ENSP00000365083.2:n.-103+1813C>T | |
| ENST00000375920.8:c.-103+1813C>T (APOM) | ENSP00000365085.4:n.-103+1813C>T | |
| NM_001256169.1:c.-103+1813C>T (APOM) | NP_001243098.1:n.-103+1813C>T | |
| NR_045828.1:n.142+1813C>T (APOM) | ||
| XM_011514895.1:c.-13-2588G>A (BAG6) | XP_011513197.1:n.-13-2588G>A | |
| XM_017011279.2:c.-13-2588G>A (BAG6) | XP_016866768.1:n.-13-2588G>A | |
| XM_024446545.1:c.-13-2588G>A (BAG6) | XP_024302313.1:n.-13-2588G>A | |
| NM_001256169.2:c.-103+1813C>T (APOM) | NP_001243098.1:n.-103+1813C>T | |
| NR_045828.2:n.148+1813C>T (APOM) |