HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22726453A>T , CM000669.2:g.22726453A>T | GRCh38 |
NC_000007.13:g.22766072A>T , CM000669.1:g.22766072A>T | GRCh37 |
NC_000007.12:g.22732597A>T | NCBI36 |
NG_011640.1:g.4307A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650428.1:n.46+1115T>A (STEAP1B) | ||
ENST00000404625.5:c.-85+195A>T (IL6) | ENSP00000385675.1:n.-85+195A>T | |
NR_131935.1:n.306T>A (IL6-AS1) | ||
XM_011515390.1:c.-85+195A>T (IL6) | XP_011513692.1:n.-85+195A>T | |
XM_011515390.2:c.-85+195A>T (IL6) | XP_011513692.1:n.-85+195A>T |