HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22726967T= , CM000669.2:g.22726967T= | GRCh38 |
NC_000007.13:g.22766586T= , CM000669.1:g.22766586T= | GRCh37 |
NC_000007.12:g.22733111T= | NCBI36 |
NG_011640.1:g.4821T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650428.1:n.46+601A= (STEAP1B) | ||
ENST00000404625.5:c.-84-212T= (IL6) | ENSP00000385675.1:n.-84-212T= | |
NR_131935.1:n.54-262A= (IL6-AS1) | ||
XM_011515390.1:c.-84-212T= (IL6) | XP_011513692.1:n.-84-212T= | |
XM_011515390.2:c.-84-212T= (IL6) | XP_011513692.1:n.-84-212T= |