HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22726447T>C , CM000669.2:g.22726447T>C | GRCh38 |
NC_000007.13:g.22766066T>C , CM000669.1:g.22766066T>C | GRCh37 |
NC_000007.12:g.22732591T>C | NCBI36 |
NG_011640.1:g.4301T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650428.1:n.46+1121A>G (STEAP1B) | ||
ENST00000404625.5:c.-85+189T>C (IL6) | ENSP00000385675.1:n.-85+189T>C | |
NR_131935.1:n.312A>G (IL6-AS1) | ||
XM_011515390.1:c.-85+189T>C (IL6) | XP_011513692.1:n.-85+189T>C | |
XM_011515390.2:c.-85+189T>C (IL6) | XP_011513692.1:n.-85+189T>C |