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