HGVS | Genome Assembly |
---|---|
NC_000007.14:g.22725837G>T , CM000669.2:g.22725837G>T | GRCh38 |
NC_000007.13:g.22765456G>T , CM000669.1:g.22765456G>T | GRCh37 |
NC_000007.12:g.22731981G>T | NCBI36 |
NG_011640.1:g.3691G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650428.1:n.46+1731C>A (STEAP1B) | ||
NR_131935.1:n.922C>A (IL6-AS1) | ||
XM_011515390.1:c.-506G>T (IL6) | XP_011513692.1:n.-506G>T |