Linked Data
gnomAD v2:
7-22766719-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727100A>G , CM000669.2:g.22727100A>G | GRCh38 |
| NC_000007.13:g.22766719A>G , CM000669.1:g.22766719A>G | GRCh37 |
| NC_000007.12:g.22733244A>G | NCBI36 |
| NG_011640.1:g.4954A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650428.1:n.46+468T>C (STEAP1B) | ||
| ENST00000404625.5:c.-84-79A>G (IL6) | ENSP00000385675.1:n.-84-79A>G | |
| NR_131935.1:n.54-395T>C (IL6-AS1) | ||
| XM_005249745.3:c.-163A>G (IL6) | XP_005249802.1:n.-163A>G | |
| XM_011515390.1:c.-84-79A>G (IL6) | XP_011513692.1:n.-84-79A>G | |
| XM_011515390.2:c.-84-79A>G (IL6) | XP_011513692.1:n.-84-79A>G |