Linked Data
dbSNP Id:
rs749592460
ExAC:
2:179482896 A / G
gnomAD v2:
2-179482896-A-G
gnomAD v4:
2-178618169-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178618169A>G , CM000664.2:g.178618169A>G | GRCh38 |
| NC_000002.11:g.179482896A>G , CM000664.1:g.179482896A>G | GRCh37 |
| NC_000002.10:g.179191141A>G | NCBI36 |
| NG_011618.3:g.217634T>C , LRG_391:g.217634T>C | |
| NG_051363.1:g.100343A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000342992.11:c.39565+20T>C (TTN) | ENSP00000343764.6:n.39565+20T>C | |
| ENST00000342175.11:c.20650+20T>C (TTN) | ENSP00000340554.6:n.20650+20T>C | |
| ENST00000359218.10:c.20449+20T>C (TTN) | ENSP00000352154.5:n.20449+20T>C | |
| ENST00000342175.10:c.20650+20T>C (TTN) | ENSP00000340554.6:n.20650+20T>C | |
| ENST00000342992.10:c.39565+20T>C (TTN) | ENSP00000343764.6:n.39565+20T>C | |
| ENST00000359218.9:c.20449+20T>C (TTN) | ENSP00000352154.5:n.20449+20T>C | |
| ENST00000460472.6:c.20074+20T>C (TTN) | ENSP00000434586.1:n.20074+20T>C | |
| ENST00000589042.5:c.47269+20T>C (TTN) MANE Select | ENSP00000467141.1:n.47269+20T>C | |
| ENST00000591111.5:c.42346+20T>C (TTN) | ENSP00000465570.1:n.42346+20T>C | |
| ENST00000615779.4:c.42346+20T>C (TTN) | ENSP00000483597.1:n.42346+20T>C | |
| NM_001256850.1:c.42346+20T>C (TTN) | NP_001243779.1:n.42346+20T>C | |
| NM_001267550.2:c.47269+20T>C (TTN) MANE Select | NP_001254479.2:n.47269+20T>C | |
| NM_003319.4:c.20074+20T>C (TTN) | NP_003310.4:n.20074+20T>C | |
| NM_133378.4:c.39565+20T>C (TTN) | NP_596869.4:n.39565+20T>C | |
| NM_133432.3:c.20449+20T>C (TTN) | NP_597676.3:n.20449+20T>C | |
| NM_133437.4:c.20650+20T>C (TTN) | NP_597681.4:n.20650+20T>C | |
| NR_038271.1:n.1605-1584A>G (TTN-AS1) | ||
| XM_011511729.1:c.46366+20T>C (TTN) | XP_011510031.1:n.46366+20T>C | |
| XM_011511730.1:c.20260+20T>C (TTN) | XP_011510032.1:n.20260+20T>C | |
| XM_011511731.1:c.20119+20T>C (TTN) | XP_011510033.1:n.20119+20T>C | |
| XM_017004819.1:c.46162+20T>C (TTN) | XP_016860308.1:n.46162+20T>C | |
| XM_017004820.1:c.41560+20T>C (TTN) | XP_016860309.1:n.41560+20T>C | |
| XM_017004821.1:c.41557+20T>C (TTN) | XP_016860310.1:n.41557+20T>C | |
| XM_017004822.1:c.38599+20T>C (TTN) | XP_016860311.1:n.38599+20T>C | |
| XM_017004823.1:c.20215+20T>C (TTN) | XP_016860312.1:n.20215+20T>C | |
| XM_024453094.1:c.41710+20T>C (TTN) | XP_024308862.1:n.41710+20T>C | |
| XM_024453095.1:c.41707+20T>C (TTN) | XP_024308863.1:n.41707+20T>C | |
| XM_024453096.1:c.41140+20T>C (TTN) | XP_024308864.1:n.41140+20T>C | |
| XM_024453097.1:c.38482+20T>C (TTN) | XP_024308865.1:n.38482+20T>C | |
| XM_024453098.1:c.38401+20T>C (TTN) | XP_024308866.1:n.38401+20T>C | |
| XM_024453099.1:c.20164+20T>C (TTN) | XP_024308867.1:n.20164+20T>C | |
| XM_024453100.1:c.10018+20T>C (TTN) | XP_024308868.1:n.10018+20T>C |