HGVS | Genome Assembly |
---|---|
NC_000007.14:g.24283586G>T , CM000669.2:g.24283586G>T | GRCh38 |
NC_000007.13:g.24323205G>T , CM000669.1:g.24323205G>T | GRCh37 |
NC_000007.12:g.24289730G>T | NCBI36 |
NG_016148.1:g.4399G>T |
HGVS | Amino-acid change | |
---|---|---|
XM_017012910.1:c.42-27887C>A | XP_016868399.1:n.42-27887C>A | |
XM_017012911.1:c.42-27887C>A | XP_016868400.1:n.42-27887C>A | |
XR_001745121.1:n.473+35771C>A | ||
XR_001745122.1:n.345-86557C>A | ||
XR_001745123.1:n.473+35771C>A | ||
XR_001745124.1:n.473+35771C>A | ||
XR_001745125.1:n.473+35771C>A | ||
XR_001745126.1:n.473+35771C>A | ||
XR_001745127.1:n.345-27887C>A | ||
XR_001745129.1:n.473+35771C>A | ||
XR_001745130.1:n.473+35771C>A | ||
XR_001745131.1:n.473+35771C>A | ||
XR_001745132.1:n.473+35771C>A |