Linked Data
ClinVar Variation Id:
364693
dbSNP Id:
rs201105262
ExAC:
9:117188496 C / T
gnomAD v2:
9-117188496-C-T
gnomAD v3:
9-114426216-C-T
gnomAD v4:
9-114426216-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114426216C>T , CM000671.2:g.114426216C>T | GRCh38 |
| NC_000009.11:g.117188496C>T , CM000671.1:g.117188496C>T | GRCh37 |
| NC_000009.10:g.116228317C>T | NCBI36 |
| NG_016700.1:g.84241G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699486.1:c.885G>A | ENSP00000514397.1:p.Ser295= | |
| ENST00000362057.4:c.1161G>A MANE Select | ENSP00000354623.3:p.Ser387= | |
| ENST00000673811.1:n.909G>A | ||
| ENST00000674036.8:c.344G>A | ||
| ENST00000265134.10:c.12G>A | ENSP00000265134.6:p.Ser4= | |
| ENST00000362057.3:c.1161G>A | ENSP00000354623.3:p.Ser387= | |
| NM_001083885.2:c.12G>A | NP_001077354.2:p.Ser4= | |
| NM_001173425.1:c.1161G>A | NP_001166896.1:p.Ser387= | |
| NM_015404.3:c.1161G>A | NP_056219.3:p.Ser387= | |
| XM_005251897.3:c.964-18198G>A | XP_005251954.2:n.964-18198G>A | |
| XM_011518484.1:c.1161G>A | XP_011516786.1:p.Ser387= | |
| XM_011518485.1:c.1161G>A | XP_011516787.1:p.Ser387= | |
| XM_011518486.1:c.1161G>A | XP_011516788.1:p.Ser387= | |
| XM_011518487.1:c.1035G>A | XP_011516789.1:p.Ser345= | |
| XM_011518488.1:c.1161G>A | XP_011516790.1:p.Ser387= | |
| XM_011518489.1:c.1161G>A | XP_011516791.1:p.Ser387= | |
| XM_011518490.1:c.1161G>A | XP_011516792.1:p.Ser387= | |
| XM_011518491.1:c.1161G>A | XP_011516793.1:p.Ser387= | |
| XM_011518492.1:c.1161G>A | XP_011516794.1:p.Ser387= | |
| XM_011518493.1:c.1161G>A | XP_011516795.1:p.Ser387= | |
| XM_011518494.1:c.1161G>A | XP_011516796.1:p.Ser387= | |
| XM_011518495.1:c.-157-1192G>A | XP_011516797.1:n.-157-1192G>A | |
| XR_929747.1:n.1869G>A | ||
| XR_929748.1:n.1869G>A | ||
| XR_929749.1:n.1869G>A | ||
| XR_929750.1:n.1869G>A | ||
| XR_929751.1:n.1869G>A | ||
| XR_929752.1:n.1869G>A | ||
| XR_929753.1:n.1869G>A | ||
| XR_929754.1:n.1869G>A | ||
| XR_929755.1:n.1869G>A | ||
| XR_929756.1:n.1869G>A | ||
| XR_929757.1:n.1869G>A | ||
| XM_011518486.2:c.1161G>A | XP_011516788.1:p.Ser387= | |
| XM_011518487.2:c.1035G>A | XP_011516789.1:p.Ser345= | |
| XM_011518488.2:c.1161G>A | XP_011516790.1:p.Ser387= | |
| XM_011518489.3:c.1161G>A | XP_011516791.1:p.Ser387= | |
| XM_011518491.3:c.1161G>A | XP_011516793.1:p.Ser387= | |
| XM_011518492.2:c.1161G>A | XP_011516794.1:p.Ser387= | |
| XM_011518494.3:c.1161G>A | XP_011516796.1:p.Ser387= | |
| XR_929747.2:n.1180G>A | ||
| XR_929748.2:n.1180G>A | ||
| XR_929749.2:n.1180G>A | ||
| XR_929750.3:n.1180G>A | ||
| XR_929752.2:n.1180G>A | ||
| XR_929753.3:n.1180G>A | ||
| XR_929754.2:n.1180G>A | ||
| XR_929755.3:n.1180G>A | ||
| XR_929756.2:n.1180G>A | ||
| XR_929757.2:n.1180G>A | ||
| NM_015404.4:c.1161G>A MANE Select | NP_056219.3:p.Ser387= | |
| NM_001173425.2:c.1161G>A | NP_001166896.1:p.Ser387= | |
| NM_001083885.3:c.12G>A | NP_001077354.2:p.Ser4= |