Linked Data
dbSNP Id:
rs1034241131
gnomAD v2:
7-22766889-CCTT-C
gnomAD v3:
7-22727270-CCTT-C
gnomAD v4:
7-22727270-CCTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727273_22727275del , CM000669.2:g.22727273_22727275del | GRCh38 |
| NC_000007.13:g.22766892_22766894del , CM000669.1:g.22766892_22766894del | GRCh37 |
| NC_000007.12:g.22733417_22733419del | NCBI36 |
| NG_011640.1:g.5127_5129del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464710.2:n.97_99del (IL6) | ||
| ENST00000258743.10:c.11_13del (IL6) MANE Select | ENSP00000258743.5:p.Phe4del | |
| ENST00000650428.1:n.46+295_46+297del (STEAP1B) | ||
| ENST00000258743.9:c.11_13del (IL6) | ENSP00000258743.5:p.Phe4del | |
| ENST00000401630.7:c.11_13del (IL6) | ENSP00000384928.3:p.Phe4del | |
| ENST00000401651.5:c.-27_-25del (IL6) | ENSP00000385718.1:n.-27_-25del | |
| ENST00000404625.5:c.11_13del (IL6) | ENSP00000385675.1:p.Phe4del | |
| ENST00000406575.1:c.11_13del (IL6) | ENSP00000385227.1:p.Phe4del | |
| ENST00000407492.5:c.-27_-25del (IL6) | ENSP00000385043.1:n.-27_-25del | |
| ENST00000426291.5:c.11_13del (IL6) | ENSP00000405150.1:p.Phe4del | |
| ENST00000485300.1:n.74_76del (IL6) | ||
| NM_000600.3:c.11_13del (IL6) | NP_000591.1:p.Phe4del | |
| NR_131935.1:n.53+295_53+297del (IL6-AS1) | ||
| XM_005249745.3:c.11_13del (IL6) | XP_005249802.1:p.Phe4del | |
| XM_011515390.1:c.11_13del (IL6) | XP_011513692.1:p.Phe4del | |
| XM_011515391.1:c.-27_-25del (IL6) | XP_011513693.1:n.-27_-25del | |
| NM_000600.4:c.11_13del (IL6) | NP_000591.1:p.Phe4del | |
| NM_001318095.1:c.-27_-25del (IL6) | NP_001305024.1:n.-27_-25del | |
| XM_005249745.5:c.11_13del (IL6) | XP_005249802.1:p.Phe4del | |
| XM_011515390.2:c.11_13del (IL6) | XP_011513692.1:p.Phe4del | |
| NM_000600.5:c.11_13del (IL6) MANE Select | NP_000591.1:p.Phe4del | |
| NM_001318095.2:c.-27_-25del (IL6) | NP_001305024.1:n.-27_-25del | |
| NM_001371096.1:c.11_13del (IL6) | NP_001358025.1:p.Phe4del |