HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10412471_10413556del , CM000682.2:g.10412471_10413556del | GRCh38 |
NC_000020.10:g.10393119_10394204del , CM000682.1:g.10393119_10394204del | GRCh37 |
NC_000020.9:g.10341119_10342204del | NCBI36 |
NG_009109.1:g.25664_26749del | |
NG_009109.2:g.25664_26749del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651692.1:c.-41_985+60del | ||
ENST00000652676.1:n.458+241_629+60del | ||
ENST00000347364.7:c.-41_985+60del | ||
ENST00000399054.6:c.-41_985+60del | ||
NM_018848.3:c.-41_985+60del | ||
NM_170784.2:c.-41_985+60del | ||
NR_072977.1:n.364-4752_364-3667del | ||
NR_072977.2:n.347-4752_347-3667del | ||
NM_170784.3:c.-41_985+60del |