HGVS | Genome Assembly |
---|---|
NC_000007.14:g.24291867A>T , CM000669.2:g.24291867A>T | GRCh38 |
NC_000007.13:g.24331486A>T , CM000669.1:g.24331486A>T | GRCh37 |
NC_000007.12:g.24298011A>T | NCBI36 |
NG_016148.1:g.12680A>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_017012910.1:c.41+27490T>A | XP_016868399.1:n.41+27490T>A | |
XM_017012911.1:c.41+27490T>A | XP_016868400.1:n.41+27490T>A | |
XR_001745121.1:n.473+27490T>A | ||
XR_001745122.1:n.345-94838T>A | ||
XR_001745123.1:n.473+27490T>A | ||
XR_001745124.1:n.473+27490T>A | ||
XR_001745125.1:n.473+27490T>A | ||
XR_001745126.1:n.473+27490T>A | ||
XR_001745127.1:n.345-36168T>A | ||
XR_001745129.1:n.473+27490T>A | ||
XR_001745130.1:n.473+27490T>A | ||
XR_001745131.1:n.473+27490T>A | ||
XR_001745132.1:n.473+27490T>A |