HGVS | Genome Assembly |
---|---|
NC_000007.14:g.24282734G>A , CM000669.2:g.24282734G>A | GRCh38 |
NC_000007.13:g.24322353G>A , CM000669.1:g.24322353G>A | GRCh37 |
NC_000007.12:g.24288878G>A | NCBI36 |
NG_016148.1:g.3547G>A |
HGVS | Amino-acid change | |
---|---|---|
XM_017012910.1:c.42-27035C>T | XP_016868399.1:n.42-27035C>T | |
XM_017012911.1:c.42-27035C>T | XP_016868400.1:n.42-27035C>T | |
XR_001745121.1:n.473+36623C>T | ||
XR_001745122.1:n.345-85705C>T | ||
XR_001745123.1:n.473+36623C>T | ||
XR_001745124.1:n.473+36623C>T | ||
XR_001745125.1:n.473+36623C>T | ||
XR_001745126.1:n.473+36623C>T | ||
XR_001745127.1:n.345-27035C>T | ||
XR_001745129.1:n.473+36623C>T | ||
XR_001745130.1:n.473+36623C>T | ||
XR_001745131.1:n.473+36623C>T | ||
XR_001745132.1:n.473+36623C>T |