Linked Data
dbSNP Id:
rs925956545
gnomAD v2:
8-100789300-C-T
gnomAD v3:
8-99777072-C-T
gnomAD v4:
8-99777072-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99777072C>T , CM000670.2:g.99777072C>T | GRCh38 |
| NC_000008.10:g.100789300C>T , CM000670.1:g.100789300C>T | GRCh37 |
| NC_000008.9:g.100858476C>T | NCBI36 |
| NG_007098.2:g.768807C>T , LRG_351:g.768807C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682153.1:c.7504+116C>T | ENSP00000507923.1:n.7504+116C>T | |
| ENST00000682358.1:n.7574+116C>T | ||
| ENST00000683334.1:c.*3186+116C>T | ENSP00000507369.1:n.*3186+116C>T | |
| ENST00000357162.7:c.7429+116C>T MANE Select | ENSP00000349685.2:n.7429+116C>T | |
| ENST00000358544.7:c.7504+116C>T MANE Plus Clinical | ENSP00000351346.2:n.7504+116C>T | |
| ENST00000357162.6:c.7429+116C>T | ENSP00000349685.2:n.7429+116C>T | |
| ENST00000358544.6:c.7504+116C>T | ENSP00000351346.2:n.7504+116C>T | |
| ENST00000518569.1:n.378-1610C>T | ||
| NM_017890.4:c.7504+116C>T , LRG_351t1:c.7504+116C>T | NP_060360.3:n.7504+116C>T | |
| NM_152564.4:c.7429+116C>T , LRG_351t2:c.7429+116C>T | NP_689777.3:n.7429+116C>T | |
| XM_005250800.2:c.7504+116C>T | XP_005250857.1:n.7504+116C>T | |
| XM_005250801.3:c.7504+116C>T | XP_005250858.1:n.7504+116C>T | |
| XM_011516848.1:c.7501+116C>T | XP_011515150.1:n.7501+116C>T | |
| XM_011516849.1:c.7426+116C>T | XP_011515151.1:n.7426+116C>T | |
| XM_011516850.1:c.7126+116C>T | XP_011515152.1:n.7126+116C>T | |
| XM_011516851.1:c.4390+116C>T | XP_011515153.1:n.4390+116C>T | |
| XM_011516852.1:c.4390+116C>T | XP_011515154.1:n.4390+116C>T | |
| XM_011516853.1:c.7504+116C>T | XP_011515155.1:n.7504+116C>T | |
| XM_011516854.1:c.3283+116C>T | XP_011515156.1:n.3283+116C>T | |
| XR_928446.1:n.1830+5406G>A | ||
| XM_005250800.3:c.7504+116C>T | XP_005250857.1:n.7504+116C>T | |
| XM_005250801.5:c.7504+116C>T | XP_005250858.1:n.7504+116C>T | |
| XM_011516848.2:c.7501+116C>T | XP_011515150.1:n.7501+116C>T | |
| XM_011516849.2:c.7426+116C>T | XP_011515151.1:n.7426+116C>T | |
| XM_011516850.2:c.7126+116C>T | XP_011515152.1:n.7126+116C>T | |
| XM_011516851.2:c.4390+116C>T | XP_011515153.1:n.4390+116C>T | |
| XM_011516852.2:c.4390+116C>T | XP_011515154.1:n.4390+116C>T | |
| XM_011516853.2:c.7504+116C>T | XP_011515155.1:n.7504+116C>T | |
| XM_011516854.2:c.3283+116C>T | XP_011515156.1:n.3283+116C>T | |
| XM_017013109.1:c.7309+116C>T | XP_016868598.1:n.7309+116C>T | |
| XM_017013111.1:c.4390+116C>T | XP_016868600.1:n.4390+116C>T | |
| XM_017013112.1:c.3061+116C>T | XP_016868601.1:n.3061+116C>T | |
| XM_024447074.1:c.6289+116C>T | XP_024302842.1:n.6289+116C>T | |
| NM_017890.5:c.7504+116C>T MANE Plus Clinical | NP_060360.3:n.7504+116C>T | |
| NM_152564.5:c.7429+116C>T MANE Select | NP_689777.3:n.7429+116C>T |