Linked Data
gnomAD v4:
7-22726999-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22726999G>A , CM000669.2:g.22726999G>A | GRCh38 |
| NC_000007.13:g.22766618G>A , CM000669.1:g.22766618G>A | GRCh37 |
| NC_000007.12:g.22733143G>A | NCBI36 |
| NG_011640.1:g.4853G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+569C>T (STEAP1B) | ||
| ENST00000404625.5:c.-84-180G>A (IL6) | ENSP00000385675.1:n.-84-180G>A | |
| NR_131935.1:n.54-294C>T (IL6-AS1) | ||
| XM_011515390.1:c.-84-180G>A (IL6) | XP_011513692.1:n.-84-180G>A | |
| XM_011515390.2:c.-84-180G>A (IL6) | XP_011513692.1:n.-84-180G>A |