Linked Data
ClinVar Variation Id:
45658
dbSNP Id:
rs139337135
ExAC:
9:117185612 G / C
gnomAD v2:
9-117185612-G-C
gnomAD v3:
9-114423332-G-C
gnomAD v4:
9-114423332-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114423332G>C , CM000671.2:g.114423332G>C | GRCh38 |
| NC_000009.11:g.117185612G>C , CM000671.1:g.117185612G>C | GRCh37 |
| NC_000009.10:g.116225433G>C | NCBI36 |
| NG_016700.1:g.87125C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699486.1:c.1332C>G | ENSP00000514397.1:p.Thr444= | |
| ENST00000362057.4:c.1608C>G MANE Select | ENSP00000354623.3:p.Thr536= | |
| ENST00000673811.1:n.2350+1002C>G | ||
| ENST00000674036.8:c.599+1002C>G | ||
| ENST00000674048.1:n.1489C>G | ||
| ENST00000265134.10:c.459C>G | ENSP00000265134.6:p.Thr153= | |
| ENST00000362057.3:c.1608C>G | ENSP00000354623.3:p.Thr536= | |
| ENST00000374059.7:c.555C>G | ENSP00000363172.3:p.Thr185= | |
| NM_001083885.2:c.459C>G | NP_001077354.2:p.Thr153= | |
| NM_001173425.1:c.1608C>G | NP_001166896.1:p.Thr536= | |
| NM_015404.3:c.1608C>G | NP_056219.3:p.Thr536= | |
| XM_005251897.3:c.964-15314C>G | XP_005251954.2:n.964-15314C>G | |
| XM_011518484.1:c.1608C>G | XP_011516786.1:p.Thr536= | |
| XM_011518485.1:c.1608C>G | XP_011516787.1:p.Thr536= | |
| XM_011518486.1:c.1608C>G | XP_011516788.1:p.Thr536= | |
| XM_011518487.1:c.1482C>G | XP_011516789.1:p.Thr494= | |
| XM_011518488.1:c.1416+1002C>G | XP_011516790.1:n.1416+1002C>G | |
| XM_011518489.1:c.1608C>G | XP_011516791.1:p.Thr536= | |
| XM_011518490.1:c.1608C>G | XP_011516792.1:p.Thr536= | |
| XM_011518491.1:c.1608C>G | XP_011516793.1:p.Thr536= | |
| XM_011518492.1:c.1608C>G | XP_011516794.1:p.Thr536= | |
| XM_011518493.1:c.1608C>G | XP_011516795.1:p.Thr536= | |
| XM_011518494.1:c.1608C>G | XP_011516796.1:p.Thr536= | |
| XM_011518495.1:c.285C>G | XP_011516797.1:p.Thr95= | |
| XR_929747.1:n.2316C>G | ||
| XR_929748.1:n.2316C>G | ||
| XR_929749.1:n.2316C>G | ||
| XR_929750.1:n.2316C>G | ||
| XR_929751.1:n.2316C>G | ||
| XR_929752.1:n.2316C>G | ||
| XR_929753.1:n.2316C>G | ||
| XR_929754.1:n.2316C>G | ||
| XR_929755.1:n.2316C>G | ||
| XR_929756.1:n.2316C>G | ||
| XR_929757.1:n.2316C>G | ||
| NM_001346890.1:c.555C>G | NP_001333819.1:p.Thr185= | |
| XM_011518486.2:c.1608C>G | XP_011516788.1:p.Thr536= | |
| XM_011518487.2:c.1482C>G | XP_011516789.1:p.Thr494= | |
| XM_011518488.2:c.1416+1002C>G | XP_011516790.1:n.1416+1002C>G | |
| XM_011518489.3:c.1608C>G | XP_011516791.1:p.Thr536= | |
| XM_011518491.3:c.1608C>G | XP_011516793.1:p.Thr536= | |
| XM_011518492.2:c.1608C>G | XP_011516794.1:p.Thr536= | |
| XM_011518494.3:c.1608C>G | XP_011516796.1:p.Thr536= | |
| XR_929747.2:n.1627C>G | ||
| XR_929748.2:n.1627C>G | ||
| XR_929749.2:n.1627C>G | ||
| XR_929750.3:n.1627C>G | ||
| XR_929752.2:n.1627C>G | ||
| XR_929753.3:n.1627C>G | ||
| XR_929754.2:n.1627C>G | ||
| XR_929755.3:n.1627C>G | ||
| XR_929756.2:n.1627C>G | ||
| XR_929757.2:n.1627C>G | ||
| NM_015404.4:c.1608C>G MANE Select | NP_056219.3:p.Thr536= | |
| NM_001173425.2:c.1608C>G | NP_001166896.1:p.Thr536= | |
| NM_001083885.3:c.459C>G | NP_001077354.2:p.Thr153= |