gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.30893055 (NFE)
Genomes Max Group AF
0.30934012 (NFE)
Exomes Max Group AF
0.13993746 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.38825904C>T , CM000666.2:g.38825904C>T | GRCh38 |
| NC_000004.11:g.38827525C>T , CM000666.1:g.38827525C>T | GRCh37 |
| NC_000004.10:g.38503920C>T | NCBI36 |
| NG_028087.1:g.35914G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508254.6:c.*1179G>A (TLR6) MANE Select | ENSP00000424718.2:n.*1179G>A | |
| ENST00000436693.6:c.*1179G>A (TLR6) | ENSP00000389600.2:n.*1179G>A | |
| ENST00000506146.5:c.-352-20711G>A (TLR1) | ENSP00000423725.1:n.-352-20711G>A | |
| NM_006068.4:c.*1179G>A (TLR6) | NP_006059.2:n.*1179G>A | |
| XM_005262637.3:c.*1179G>A (TLR6) | XP_005262694.1:n.*1179G>A | |
| XM_011513612.1:c.*1179G>A (TLR6) | XP_011511914.1:n.*1179G>A | |
| XM_011513613.1:c.*1179G>A (TLR6) | XP_011511915.1:n.*1179G>A | |
| XM_011513614.1:c.*1179G>A (TLR6) | XP_011511916.1:n.*1179G>A | |
| XM_005262637.5:c.*1179G>A (TLR6) | XP_005262694.1:n.*1179G>A | |
| XM_011513613.3:c.*1179G>A (TLR6) | XP_011511915.1:n.*1179G>A | |
| XM_011513614.3:c.*1179G>A (TLR6) | XP_011511916.1:n.*1179G>A | |
| XM_024453873.1:c.*1179G>A (TLR6) | XP_024309641.1:n.*1179G>A | |
| NM_006068.5:c.*1179G>A (TLR6) MANE Select | NP_006059.2:n.*1179G>A | |
| NM_001394553.1:c.*1179G>A (TLR6) | NP_001381482.1:n.*1179G>A |