Linked Data
ClinVar Variation Id:
47738
dbSNP Id:
rs116593093
ExAC:
2:179615386 G / C
gnomAD v2:
2-179615386-G-C
gnomAD v3:
2-178750659-G-C
gnomAD v4:
2-178750659-G-C
PubMed:
PMID:23861362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178750659G>C , CM000664.2:g.178750659G>C | GRCh38 |
| NC_000002.11:g.179615386G>C , CM000664.1:g.179615386G>C | GRCh37 |
| NC_000002.10:g.179323631G>C | NCBI36 |
| NG_011618.3:g.85144C>G , LRG_391:g.85144C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000342992.11:c.10360+2465C>G | ENSP00000343764.6:n.10360+2465C>G | |
| ENST00000342175.11:c.10798+2465C>G | ENSP00000340554.6:n.10798+2465C>G | |
| ENST00000359218.10:c.10597+2465C>G | ENSP00000352154.5:n.10597+2465C>G | |
| ENST00000360870.10:c.11741C>G MANE Plus Clinical | ENSP00000354117.4:p.Thr3914Arg | |
| ENST00000342175.10:c.10798+2465C>G | ENSP00000340554.6:n.10798+2465C>G | |
| ENST00000342992.10:c.10360+2465C>G | ENSP00000343764.6:n.10360+2465C>G | |
| ENST00000359218.9:c.10597+2465C>G | ENSP00000352154.5:n.10597+2465C>G | |
| ENST00000360870.9:c.11741C>G | ENSP00000354117.4:p.Thr3914Arg | |
| ENST00000460472.6:c.10222+2465C>G | ENSP00000434586.1:n.10222+2465C>G | |
| ENST00000589042.5:c.11311+2465C>G MANE Select | ENSP00000467141.1:n.11311+2465C>G | |
| ENST00000591111.5:c.10360+2465C>G | ENSP00000465570.1:n.10360+2465C>G | |
| ENST00000615779.4:c.10360+2465C>G | ENSP00000483597.1:n.10360+2465C>G | |
| NM_001256850.1:c.10360+2465C>G | NP_001243779.1:n.10360+2465C>G | |
| NM_001267550.2:c.11311+2465C>G MANE Select | NP_001254479.2:n.11311+2465C>G | |
| NM_003319.4:c.10222+2465C>G | NP_003310.4:n.10222+2465C>G | |
| NM_133378.4:c.10360+2465C>G | NP_596869.4:n.10360+2465C>G | |
| NM_133379.4:c.11741C>G , LRG_391t2:c.11741C>G | NP_596870.2:p.Thr3914Arg | |
| NM_133432.3:c.10597+2465C>G | NP_597676.3:n.10597+2465C>G | |
| NM_133437.4:c.10798+2465C>G | NP_597681.4:n.10798+2465C>G | |
| XM_011511729.1:c.10408+2465C>G | XP_011510031.1:n.10408+2465C>G | |
| XM_011511730.1:c.10408+2465C>G | XP_011510032.1:n.10408+2465C>G | |
| XM_011511731.1:c.10267+2465C>G | XP_011510033.1:n.10267+2465C>G | |
| XM_011511732.1:c.11786C>G | XP_011510034.1:p.Thr3929Arg | |
| XM_017004819.1:c.10363+2465C>G | XP_016860308.1:n.10363+2465C>G | |
| XM_017004820.1:c.10363+2465C>G | XP_016860309.1:n.10363+2465C>G | |
| XM_017004821.1:c.10360+2465C>G | XP_016860310.1:n.10360+2465C>G | |
| XM_017004822.1:c.10363+2465C>G | XP_016860311.1:n.10363+2465C>G | |
| XM_017004823.1:c.10363+2465C>G | XP_016860312.1:n.10363+2465C>G | |
| XM_024453094.1:c.10363+2465C>G | XP_024308862.1:n.10363+2465C>G | |
| XM_024453095.1:c.10363+2465C>G | XP_024308863.1:n.10363+2465C>G | |
| XM_024453096.1:c.10363+2465C>G | XP_024308864.1:n.10363+2465C>G | |
| XM_024453097.1:c.10363+2465C>G | XP_024308865.1:n.10363+2465C>G | |
| XM_024453098.1:c.10363+2465C>G | XP_024308866.1:n.10363+2465C>G | |
| XM_024453099.1:c.10363+2465C>G | XP_024308867.1:n.10363+2465C>G | |
| NM_133379.5:c.11741C>G MANE Plus Clinical | NP_596870.2:p.Thr3914Arg |