Linked Data
gnomAD v4:
7-22727097-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22727098del , CM000669.2:g.22727098del | GRCh38 |
| NC_000007.13:g.22766717del , CM000669.1:g.22766717del | GRCh37 |
| NC_000007.12:g.22733242del | NCBI36 |
| NG_011640.1:g.4952del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+470del (STEAP1B) | ||
| ENST00000404625.5:c.-84-81del (IL6) | ENSP00000385675.1:n.-84-81del | |
| NR_131935.1:n.54-393del (IL6-AS1) | ||
| XM_005249745.3:c.-165del (IL6) | XP_005249802.1:n.-165del | |
| XM_011515390.1:c.-84-81del (IL6) | XP_011513692.1:n.-84-81del | |
| XM_011515390.2:c.-84-81del (IL6) | XP_011513692.1:n.-84-81del |