Linked Data
ClinVar Variation Id:
1338320
dbSNP Id:
rs143787982
ExAC:
8:100831746 G / A
gnomAD v2:
8-100831746-G-A
gnomAD v3:
8-99819518-G-A
gnomAD v4:
8-99819518-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99819518G>A , CM000670.2:g.99819518G>A | GRCh38 |
| NC_000008.10:g.100831746G>A , CM000670.1:g.100831746G>A | GRCh37 |
| NC_000008.9:g.100900922G>A | NCBI36 |
| NG_007098.2:g.811253G>A , LRG_351:g.811253G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682153.1:c.8803G>A | ENSP00000507923.1:p.Glu2935Lys | |
| ENST00000682358.1:n.8873G>A | ||
| ENST00000683334.1:c.*4485G>A | ENSP00000507369.1:n.*4485G>A | |
| ENST00000357162.7:c.8728G>A MANE Select | ENSP00000349685.2:p.Glu2910Lys | |
| ENST00000358544.7:c.8803G>A MANE Plus Clinical | ENSP00000351346.2:p.Glu2935Lys | |
| ENST00000357162.6:c.8728G>A | ENSP00000349685.2:p.Glu2910Lys | |
| ENST00000358544.6:c.8803G>A | ENSP00000351346.2:p.Glu2935Lys | |
| NM_017890.4:c.8803G>A , LRG_351t1:c.8803G>A | NP_060360.3:p.Glu2935Lys | |
| NM_152564.4:c.8728G>A , LRG_351t2:c.8728G>A | NP_689777.3:p.Glu2910Lys | |
| XM_005250800.2:c.8803G>A | XP_005250857.1:p.Glu2935Lys | |
| XM_005250801.3:c.8803G>A | XP_005250858.1:p.Glu2935Lys | |
| XM_011516848.1:c.8800G>A | XP_011515150.1:p.Glu2934Lys | |
| XM_011516849.1:c.8725G>A | XP_011515151.1:p.Glu2909Lys | |
| XM_011516850.1:c.8425G>A | XP_011515152.1:p.Glu2809Lys | |
| XM_011516851.1:c.5689G>A | XP_011515153.1:p.Glu1897Lys | |
| XM_011516852.1:c.5689G>A | XP_011515154.1:p.Glu1897Lys | |
| XM_011516854.1:c.4582G>A | XP_011515156.1:p.Glu1528Lys | |
| XM_005250800.3:c.8803G>A | XP_005250857.1:p.Glu2935Lys | |
| XM_005250801.5:c.8803G>A | XP_005250858.1:p.Glu2935Lys | |
| XM_011516848.2:c.8800G>A | XP_011515150.1:p.Glu2934Lys | |
| XM_011516849.2:c.8725G>A | XP_011515151.1:p.Glu2909Lys | |
| XM_011516850.2:c.8425G>A | XP_011515152.1:p.Glu2809Lys | |
| XM_011516851.2:c.5689G>A | XP_011515153.1:p.Glu1897Lys | |
| XM_011516852.2:c.5689G>A | XP_011515154.1:p.Glu1897Lys | |
| XM_011516854.2:c.4582G>A | XP_011515156.1:p.Glu1528Lys | |
| XM_017013109.1:c.8608G>A | XP_016868598.1:p.Glu2870Lys | |
| XM_017013111.1:c.5689G>A | XP_016868600.1:p.Glu1897Lys | |
| XM_017013112.1:c.4360G>A | XP_016868601.1:p.Glu1454Lys | |
| XM_024447074.1:c.7588G>A | XP_024302842.1:p.Glu2530Lys | |
| NM_017890.5:c.8803G>A MANE Plus Clinical | NP_060360.3:p.Glu2935Lys | |
| NM_152564.5:c.8728G>A MANE Select | NP_689777.3:p.Glu2910Lys |