MyVariant.info:
GRCh37
chr2:g.179479368A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178614641A>G , CM000664.2:g.178614641A>G | GRCh38 |
| NC_000002.11:g.179479368A>G , CM000664.1:g.179479368A>G | GRCh37 |
| NC_000002.10:g.179187613A>G | NCBI36 |
| NG_011618.3:g.221162T>C , LRG_391:g.221162T>C | |
| NG_051363.1:g.96815A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.41169T>C (TTN) | ENSP00000343764.6:p.Thr13723= | |
| ENST00000342175.11:c.22254T>C (TTN) | ENSP00000340554.6:p.Thr7418= | |
| ENST00000359218.10:c.22053T>C (TTN) | ENSP00000352154.5:p.Thr7351= | |
| ENST00000342175.10:c.22254T>C (TTN) | ENSP00000340554.6:p.Thr7418= | |
| ENST00000342992.10:c.41169T>C (TTN) | ENSP00000343764.6:p.Thr13723= | |
| ENST00000359218.9:c.22053T>C (TTN) | ENSP00000352154.5:p.Thr7351= | |
| ENST00000460472.6:c.21678T>C (TTN) | ENSP00000434586.1:p.Thr7226= | |
| ENST00000589042.5:c.48873T>C (TTN) MANE Select | ENSP00000467141.1:p.Thr16291= | |
| ENST00000591111.5:c.43950T>C (TTN) | ENSP00000465570.1:p.Thr14650= | |
| ENST00000615779.4:c.43950T>C (TTN) | ENSP00000483597.1:p.Thr14650= | |
| NM_001256850.1:c.43950T>C (TTN) | NP_001243779.1:p.Thr14650= | |
| NM_001267550.2:c.48873T>C (TTN) MANE Select | NP_001254479.2:p.Thr16291= | |
| NM_003319.4:c.21678T>C (TTN) | NP_003310.4:p.Thr7226= | |
| NM_133378.4:c.41169T>C (TTN) | NP_596869.4:p.Thr13723= | |
| NM_133432.3:c.22053T>C (TTN) | NP_597676.3:p.Thr7351= | |
| NM_133437.4:c.22254T>C (TTN) | NP_597681.4:p.Thr7418= | |
| NR_038271.1:n.1389A>G (TTN-AS1) | ||
| XM_011511729.1:c.47970T>C (TTN) | XP_011510031.1:p.Thr15990= | |
| XM_011511730.1:c.21864T>C (TTN) | XP_011510032.1:p.Thr7288= | |
| XM_011511731.1:c.21723T>C (TTN) | XP_011510033.1:p.Thr7241= | |
| XM_017004819.1:c.47766T>C (TTN) | XP_016860308.1:p.Thr15922= | |
| XM_017004820.1:c.43164T>C (TTN) | XP_016860309.1:p.Thr14388= | |
| XM_017004821.1:c.43161T>C (TTN) | XP_016860310.1:p.Thr14387= | |
| XM_017004822.1:c.40203T>C (TTN) | XP_016860311.1:p.Thr13401= | |
| XM_017004823.1:c.21819T>C (TTN) | XP_016860312.1:p.Thr7273= | |
| XM_024453094.1:c.43314T>C (TTN) | XP_024308862.1:p.Thr14438= | |
| XM_024453095.1:c.43311T>C (TTN) | XP_024308863.1:p.Thr14437= | |
| XM_024453096.1:c.42744T>C (TTN) | XP_024308864.1:p.Thr14248= | |
| XM_024453097.1:c.40086T>C (TTN) | XP_024308865.1:p.Thr13362= | |
| XM_024453098.1:c.40005T>C (TTN) | XP_024308866.1:p.Thr13335= | |
| XM_024453099.1:c.21768T>C (TTN) | XP_024308867.1:p.Thr7256= | |
| XM_024453100.1:c.11622T>C (TTN) | XP_024308868.1:p.Thr3874= |