HGVS | Genome Assembly |
---|---|
NC_000017.11:g.27801555C>A , CM000679.2:g.27801555C>A | GRCh38 |
NC_000017.10:g.26128581C>A , CM000679.1:g.26128581C>A | GRCh37 |
NC_000017.9:g.23152708C>A | NCBI36 |
NG_011470.1:g.3975G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000582441.1:c.438+2568G>T | ENSP00000462879.1:n.438+2568G>T | |
XM_011524859.1:c.-74+2568G>T | XP_011523161.1:n.-74+2568G>T |