HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73420322del , CM000666.2:g.73420322del | GRCh38 |
NC_000004.11:g.74286039del , CM000666.1:g.74286039del | GRCh37 |
NC_000004.10:g.74504903del | NCBI36 |
NG_009291.1:g.21068del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295897.9:c.*23+1del | ||
ENST00000295897.8:c.*23+1del | ||
ENST00000401494.7:c.*23+1del | ||
ENST00000415165.6:c.*23+1del | ||
ENST00000476441.6:c.*1132+1del | ||
ENST00000495173.1:n.161+1del | ||
ENST00000503124.5:c.*23+1del | ||
ENST00000505649.5:n.1400+1del | ||
ENST00000508932.5:n.243+1del | ||
ENST00000509063.5:c.1785+683del | ENSP00000422784.1:n.1785+683del | |
ENST00000511370.1:c.1386+1del | ||
ENST00000621085.4:c.*23+1del | ||
ENST00000621628.4:c.*23+1del | ||
NM_000477.5:c.*23+1del | ||
NM_000477.6:c.*23+1del | ||
NM_000477.7:c.*23+1del |