Linked Data
ClinVar Variation Id:
664625
ClinVar RCV Id:
RCV000822753
dbSNP Id:
rs749392832
ExAC:
8:100880519 G / A
gnomAD v2:
8-100880519-G-A
gnomAD v4:
8-99868291-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99868291G>A , CM000670.2:g.99868291G>A | GRCh38 |
| NC_000008.10:g.100880519G>A , CM000670.1:g.100880519G>A | GRCh37 |
| NC_000008.9:g.100949695G>A | NCBI36 |
| NG_007098.2:g.860026G>A , LRG_351:g.860026G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682153.1:c.*387G>A | ENSP00000507923.1:n.*387G>A | |
| ENST00000682358.1:n.11363G>A | ||
| ENST00000683334.1:c.*6975G>A | ENSP00000507369.1:n.*6975G>A | |
| ENST00000357162.7:c.11218G>A MANE Select | ENSP00000349685.2:p.Ala3740Thr | |
| ENST00000358544.7:c.11293G>A MANE Plus Clinical | ENSP00000351346.2:p.Ala3765Thr | |
| ENST00000357162.6:c.11218G>A | ENSP00000349685.2:p.Ala3740Thr | |
| ENST00000358544.6:c.11293G>A | ENSP00000351346.2:p.Ala3765Thr | |
| ENST00000493587.1:n.235G>A | ||
| NM_017890.4:c.11293G>A , LRG_351t1:c.11293G>A | NP_060360.3:p.Ala3765Thr | |
| NM_152564.4:c.11218G>A , LRG_351t2:c.11218G>A | NP_689777.3:p.Ala3740Thr | |
| XM_005250800.2:c.11293G>A | XP_005250857.1:p.Ala3765Thr | |
| XM_005250801.3:c.11293G>A | XP_005250858.1:p.Ala3765Thr | |
| XM_011516848.1:c.11290G>A | XP_011515150.1:p.Ala3764Thr | |
| XM_011516849.1:c.11215G>A | XP_011515151.1:p.Ala3739Thr | |
| XM_011516850.1:c.10915G>A | XP_011515152.1:p.Ala3639Thr | |
| XM_011516851.1:c.8179G>A | XP_011515153.1:p.Ala2727Thr | |
| XM_011516852.1:c.8179G>A | XP_011515154.1:p.Ala2727Thr | |
| XM_011516854.1:c.7072G>A | XP_011515156.1:p.Ala2358Thr | |
| XM_005250800.3:c.11293G>A | XP_005250857.1:p.Ala3765Thr | |
| XM_005250801.5:c.11293G>A | XP_005250858.1:p.Ala3765Thr | |
| XM_011516848.2:c.11290G>A | XP_011515150.1:p.Ala3764Thr | |
| XM_011516849.2:c.11215G>A | XP_011515151.1:p.Ala3739Thr | |
| XM_011516850.2:c.10915G>A | XP_011515152.1:p.Ala3639Thr | |
| XM_011516851.2:c.8179G>A | XP_011515153.1:p.Ala2727Thr | |
| XM_011516852.2:c.8179G>A | XP_011515154.1:p.Ala2727Thr | |
| XM_011516854.2:c.7072G>A | XP_011515156.1:p.Ala2358Thr | |
| XM_017013109.1:c.11098G>A | XP_016868598.1:p.Ala3700Thr | |
| XM_017013111.1:c.8179G>A | XP_016868600.1:p.Ala2727Thr | |
| XM_017013112.1:c.6850G>A | XP_016868601.1:p.Ala2284Thr | |
| XM_024447074.1:c.10078G>A | XP_024302842.1:p.Ala3360Thr | |
| NM_017890.5:c.11293G>A MANE Plus Clinical | NP_060360.3:p.Ala3765Thr | |
| NM_152564.5:c.11218G>A MANE Select | NP_689777.3:p.Ala3740Thr |