HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22727143T>A , CM000669.2:g.22727143T>A | GRCh38 |
NC_000007.13:g.22766762T>A , CM000669.1:g.22766762T>A | GRCh37 |
NC_000007.12:g.22733287T>A | NCBI36 |
NG_011640.1:g.4997T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650428.1:n.46+425A>T (STEAP1B) | ||
ENST00000404625.5:c.-84-36T>A (IL6) | ENSP00000385675.1:n.-84-36T>A | |
NR_131935.1:n.53+425A>T (IL6-AS1) | ||
XM_005249745.3:c.-120T>A (IL6) | XP_005249802.1:n.-120T>A | |
XM_011515390.1:c.-84-36T>A (IL6) | XP_011513692.1:n.-84-36T>A | |
NM_000600.4:c.-120T>A (IL6) | NP_000591.1:n.-120T>A | |
NM_001318095.1:c.-157T>A (IL6) | NP_001305024.1:n.-157T>A | |
XM_011515390.2:c.-84-36T>A (IL6) | XP_011513692.1:n.-84-36T>A |