HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22727127G>A , CM000669.2:g.22727127G>A | GRCh38 |
NC_000007.13:g.22766746G>A , CM000669.1:g.22766746G>A | GRCh37 |
NC_000007.12:g.22733271G>A | NCBI36 |
NG_011640.1:g.4981G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650428.1:n.46+441C>T (STEAP1B) | ||
ENST00000404625.5:c.-84-52G>A (IL6) | ENSP00000385675.1:n.-84-52G>A | |
NR_131935.1:n.54-422C>T (IL6-AS1) | ||
XM_005249745.3:c.-136G>A (IL6) | XP_005249802.1:n.-136G>A | |
XM_011515390.1:c.-84-52G>A (IL6) | XP_011513692.1:n.-84-52G>A | |
XM_011515390.2:c.-84-52G>A (IL6) | XP_011513692.1:n.-84-52G>A |