HGVS | Genome Assembly |
---|---|
NC_000017.11:g.27804217C>A , CM000679.2:g.27804217C>A | GRCh38 |
NC_000017.10:g.26131243C>A , CM000679.1:g.26131243C>A | GRCh37 |
NC_000017.9:g.23155370C>A | NCBI36 |
NG_011470.1:g.1313G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000582441.1:c.344G>T | ENSP00000462879.1:p.Gly115Val | |
XM_011524859.1:c.-168G>T | XP_011523161.1:n.-168G>T |