Linked Data
dbSNP Id:
rs1389636465
gnomAD v2:
7-22766730-A-G
gnomAD v3:
7-22727111-A-G
gnomAD v4:
7-22727111-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727111A>G , CM000669.2:g.22727111A>G | GRCh38 |
| NC_000007.13:g.22766730A>G , CM000669.1:g.22766730A>G | GRCh37 |
| NC_000007.12:g.22733255A>G | NCBI36 |
| NG_011640.1:g.4965A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650428.1:n.46+457T>C (STEAP1B) | ||
| ENST00000404625.5:c.-84-68A>G (IL6) | ENSP00000385675.1:n.-84-68A>G | |
| NR_131935.1:n.54-406T>C (IL6-AS1) | ||
| XM_005249745.3:c.-152A>G (IL6) | XP_005249802.1:n.-152A>G | |
| XM_011515390.1:c.-84-68A>G (IL6) | XP_011513692.1:n.-84-68A>G | |
| XM_011515390.2:c.-84-68A>G (IL6) | XP_011513692.1:n.-84-68A>G |