HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22727132T>G , CM000669.2:g.22727132T>G | GRCh38 |
NC_000007.13:g.22766751T>G , CM000669.1:g.22766751T>G | GRCh37 |
NC_000007.12:g.22733276T>G | NCBI36 |
NG_011640.1:g.4986T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650428.1:n.46+436A>C (STEAP1B) | ||
ENST00000404625.5:c.-84-47T>G (IL6) | ENSP00000385675.1:n.-84-47T>G | |
NR_131935.1:n.54-427A>C (IL6-AS1) | ||
XM_005249745.3:c.-131T>G (IL6) | XP_005249802.1:n.-131T>G | |
XM_011515390.1:c.-84-47T>G (IL6) | XP_011513692.1:n.-84-47T>G | |
XM_011515390.2:c.-84-47T>G (IL6) | XP_011513692.1:n.-84-47T>G |