Linked Data
dbSNP Id:
rs185230192
gnomAD v2:
7-22766838-C-G
gnomAD v4:
7-22727219-C-G
MyVariant Identifiers:
chr7:g.22766838_22766839delinsGG (hg19)
chr7:g.22727219_22727220delinsGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727219C>G , CM000669.2:g.22727219C>G | GRCh38 |
| NC_000007.13:g.22766838C>G , CM000669.1:g.22766838C>G | GRCh37 |
| NC_000007.12:g.22733363C>G | NCBI36 |
| NG_011640.1:g.5073C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464710.2:n.43C>G (IL6) | ||
| ENST00000258743.10:c.-44C>G (IL6) MANE Select | ENSP00000258743.5:n.-44C>G | |
| ENST00000650428.1:n.46+349G>C (STEAP1B) | ||
| ENST00000258743.9:c.-44C>G (IL6) | ENSP00000258743.5:n.-44C>G | |
| ENST00000401651.5:c.-81C>G (IL6) | ENSP00000385718.1:n.-81C>G | |
| ENST00000404625.5:c.-44C>G (IL6) | ENSP00000385675.1:n.-44C>G | |
| ENST00000407492.5:c.-81C>G (IL6) | ENSP00000385043.1:n.-81C>G | |
| ENST00000426291.5:c.-44C>G (IL6) | ENSP00000405150.1:n.-44C>G | |
| ENST00000485300.1:n.20C>G (IL6) | ||
| NM_000600.3:c.-44C>G (IL6) | NP_000591.1:n.-44C>G | |
| NR_131935.1:n.53+349G>C (IL6-AS1) | ||
| XM_005249745.3:c.-44C>G (IL6) | XP_005249802.1:n.-44C>G | |
| XM_011515390.1:c.-44C>G (IL6) | XP_011513692.1:n.-44C>G | |
| XM_011515391.1:c.-81C>G (IL6) | XP_011513693.1:n.-81C>G | |
| NM_000600.4:c.-44C>G (IL6) | NP_000591.1:n.-44C>G | |
| NM_001318095.1:c.-81C>G (IL6) | NP_001305024.1:n.-81C>G | |
| XM_005249745.5:c.-44C>G (IL6) | XP_005249802.1:n.-44C>G | |
| XM_011515390.2:c.-44C>G (IL6) | XP_011513692.1:n.-44C>G | |
| NM_000600.5:c.-44C>G (IL6) MANE Select | NP_000591.1:n.-44C>G | |
| NM_001318095.2:c.-81C>G (IL6) | NP_001305024.1:n.-81C>G | |
| NM_001371096.1:c.-44C>G (IL6) | NP_001358025.1:n.-44C>G |