HGVS | Genome Assembly |
---|---|
NC_000007.14:g.24283715G>A , CM000669.2:g.24283715G>A | GRCh38 |
NC_000007.13:g.24323334G>A , CM000669.1:g.24323334G>A | GRCh37 |
NC_000007.12:g.24289859G>A | NCBI36 |
NG_016148.1:g.4528G>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_017012910.1:c.42-28016C>T | XP_016868399.1:n.42-28016C>T | |
XM_017012911.1:c.42-28016C>T | XP_016868400.1:n.42-28016C>T | |
XR_001745121.1:n.473+35642C>T | ||
XR_001745122.1:n.345-86686C>T | ||
XR_001745123.1:n.473+35642C>T | ||
XR_001745124.1:n.473+35642C>T | ||
XR_001745125.1:n.473+35642C>T | ||
XR_001745126.1:n.473+35642C>T | ||
XR_001745127.1:n.345-28016C>T | ||
XR_001745129.1:n.473+35642C>T | ||
XR_001745130.1:n.473+35642C>T | ||
XR_001745131.1:n.473+35642C>T | ||
XR_001745132.1:n.473+35642C>T |