Linked Data
dbSNP Id:
rs1485376559
gnomAD v2:
7-22767131-G-A
gnomAD v3:
7-22727512-G-A
gnomAD v4:
7-22727512-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727512G>A , CM000669.2:g.22727512G>A | GRCh38 |
| NC_000007.13:g.22767131G>A , CM000669.1:g.22767131G>A | GRCh37 |
| NC_000007.12:g.22733656G>A | NCBI36 |
| NG_011640.1:g.5366G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464710.2:n.336G>A (IL6) | ||
| ENST00000258743.10:c.88G>A (IL6) MANE Select | ENSP00000258743.5:p.Val30Ile | |
| ENST00000650428.1:n.46+56C>T (STEAP1B) | ||
| ENST00000258743.9:c.88G>A (IL6) | ENSP00000258743.5:p.Val30Ile | |
| ENST00000401630.7:c.20-1G>A (IL6) | ENSP00000384928.3:n.20-1G>A | |
| ENST00000401651.5:c.-19+231G>A (IL6) | ENSP00000385718.1:n.-19+231G>A | |
| ENST00000404625.5:c.88G>A (IL6) | ENSP00000385675.1:p.Val30Ile | |
| ENST00000406575.1:c.88G>A (IL6) | ENSP00000385227.1:p.Val30Ile | |
| ENST00000407492.5:c.-19+231G>A (IL6) | ENSP00000385043.1:n.-19+231G>A | |
| ENST00000426291.5:c.88G>A (IL6) | ENSP00000405150.1:p.Val30Ile | |
| ENST00000485300.1:n.313G>A (IL6) | ||
| NM_000600.3:c.88G>A (IL6) | NP_000591.1:p.Val30Ile | |
| NR_131935.1:n.53+56C>T (IL6-AS1) | ||
| XM_005249745.3:c.250G>A (IL6) | XP_005249802.1:p.Val84Ile | |
| XM_011515390.1:c.88G>A (IL6) | XP_011513692.1:p.Val30Ile | |
| XM_011515391.1:c.-19+231G>A (IL6) | XP_011513693.1:n.-19+231G>A | |
| NM_000600.4:c.88G>A (IL6) | NP_000591.1:p.Val30Ile | |
| NM_001318095.1:c.-19+231G>A (IL6) | NP_001305024.1:n.-19+231G>A | |
| XM_005249745.5:c.250G>A (IL6) | XP_005249802.1:p.Val84Ile | |
| XM_011515390.2:c.88G>A (IL6) | XP_011513692.1:p.Val30Ile | |
| NM_000600.5:c.88G>A (IL6) MANE Select | NP_000591.1:p.Val30Ile | |
| NM_001318095.2:c.-19+231G>A (IL6) | NP_001305024.1:n.-19+231G>A | |
| NM_001371096.1:c.20-1G>A (IL6) | NP_001358025.1:n.20-1G>A |