Linked Data
ClinVar Variation Id:
45642
dbSNP Id:
rs149558159
ExAC:
9:117188508 G / A
gnomAD v2:
9-117188508-G-A
gnomAD v3:
9-114426228-G-A
gnomAD v4:
9-114426228-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114426228G>A , CM000671.2:g.114426228G>A | GRCh38 |
| NC_000009.11:g.117188508G>A , CM000671.1:g.117188508G>A | GRCh37 |
| NC_000009.10:g.116228329G>A | NCBI36 |
| NG_016700.1:g.84229C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699486.1:c.873C>T | ENSP00000514397.1:p.Thr291= | |
| ENST00000362057.4:c.1149C>T MANE Select | ENSP00000354623.3:p.Thr383= | |
| ENST00000673811.1:n.897C>T | ||
| ENST00000674036.8:c.332C>T | ||
| ENST00000265134.10:c.-1C>T | ENSP00000265134.6:n.-1C>T | |
| ENST00000362057.3:c.1149C>T | ENSP00000354623.3:p.Thr383= | |
| NM_001083885.2:c.-1C>T | NP_001077354.2:n.-1C>T | |
| NM_001173425.1:c.1149C>T | NP_001166896.1:p.Thr383= | |
| NM_015404.3:c.1149C>T | NP_056219.3:p.Thr383= | |
| XM_005251897.3:c.964-18210C>T | XP_005251954.2:n.964-18210C>T | |
| XM_011518484.1:c.1149C>T | XP_011516786.1:p.Thr383= | |
| XM_011518485.1:c.1149C>T | XP_011516787.1:p.Thr383= | |
| XM_011518486.1:c.1149C>T | XP_011516788.1:p.Thr383= | |
| XM_011518487.1:c.1023C>T | XP_011516789.1:p.Thr341= | |
| XM_011518488.1:c.1149C>T | XP_011516790.1:p.Thr383= | |
| XM_011518489.1:c.1149C>T | XP_011516791.1:p.Thr383= | |
| XM_011518490.1:c.1149C>T | XP_011516792.1:p.Thr383= | |
| XM_011518491.1:c.1149C>T | XP_011516793.1:p.Thr383= | |
| XM_011518492.1:c.1149C>T | XP_011516794.1:p.Thr383= | |
| XM_011518493.1:c.1149C>T | XP_011516795.1:p.Thr383= | |
| XM_011518494.1:c.1149C>T | XP_011516796.1:p.Thr383= | |
| XM_011518495.1:c.-157-1204C>T | XP_011516797.1:n.-157-1204C>T | |
| XR_929747.1:n.1857C>T | ||
| XR_929748.1:n.1857C>T | ||
| XR_929749.1:n.1857C>T | ||
| XR_929750.1:n.1857C>T | ||
| XR_929751.1:n.1857C>T | ||
| XR_929752.1:n.1857C>T | ||
| XR_929753.1:n.1857C>T | ||
| XR_929754.1:n.1857C>T | ||
| XR_929755.1:n.1857C>T | ||
| XR_929756.1:n.1857C>T | ||
| XR_929757.1:n.1857C>T | ||
| XM_011518486.2:c.1149C>T | XP_011516788.1:p.Thr383= | |
| XM_011518487.2:c.1023C>T | XP_011516789.1:p.Thr341= | |
| XM_011518488.2:c.1149C>T | XP_011516790.1:p.Thr383= | |
| XM_011518489.3:c.1149C>T | XP_011516791.1:p.Thr383= | |
| XM_011518491.3:c.1149C>T | XP_011516793.1:p.Thr383= | |
| XM_011518492.2:c.1149C>T | XP_011516794.1:p.Thr383= | |
| XM_011518494.3:c.1149C>T | XP_011516796.1:p.Thr383= | |
| XR_929747.2:n.1168C>T | ||
| XR_929748.2:n.1168C>T | ||
| XR_929749.2:n.1168C>T | ||
| XR_929750.3:n.1168C>T | ||
| XR_929752.2:n.1168C>T | ||
| XR_929753.3:n.1168C>T | ||
| XR_929754.2:n.1168C>T | ||
| XR_929755.3:n.1168C>T | ||
| XR_929756.2:n.1168C>T | ||
| XR_929757.2:n.1168C>T | ||
| NM_015404.4:c.1149C>T MANE Select | NP_056219.3:p.Thr383= | |
| NM_001173425.2:c.1149C>T | NP_001166896.1:p.Thr383= | |
| NM_001083885.3:c.-1C>T | NP_001077354.2:n.-1C>T |