HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22726640G>T , CM000669.2:g.22726640G>T | GRCh38 |
NC_000007.13:g.22766259G>T , CM000669.1:g.22766259G>T | GRCh37 |
NC_000007.12:g.22732784G>T | NCBI36 |
NG_011640.1:g.4494G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650428.1:n.46+928C>A (STEAP1B) | ||
ENST00000404625.5:c.-85+382G>T (IL6) | ENSP00000385675.1:n.-85+382G>T | |
NR_131935.1:n.119C>A (IL6-AS1) | ||
XM_011515390.1:c.-85+382G>T (IL6) | XP_011513692.1:n.-85+382G>T | |
XM_011515390.2:c.-85+382G>T (IL6) | XP_011513692.1:n.-85+382G>T |