HGVS | Genome Assembly |
---|---|
NC_000002.12:g.223998117del , CM000664.2:g.223998117del | GRCh38 |
NC_000002.11:g.224862834del , CM000664.1:g.224862834del | GRCh37 |
NC_000002.10:g.224571078del | NCBI36 |
NG_032907.1:g.46206del | |
NG_032907.2:g.46206del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258405.9:c.487+1del | ||
ENST00000409304.6:c.487+1del | ||
ENST00000258405.8:c.487+1del | ||
ENST00000409304.5:c.487+1del | ||
ENST00000409840.7:c.487+1del | ||
ENST00000432738.5:c.487+1del | ||
ENST00000447280.6:c.523+1del | ||
NM_001136528.1:c.487+1del | ||
NM_001136530.1:c.523+1del | ||
NM_006216.3:c.487+1del | ||
NR_073116.1:n.1148+1del | ||
XM_005246641.2:c.523+1del | ||
XM_005246642.2:c.487+1del | ||
XM_017004330.1:c.487+1del | ||
XM_017004332.2:c.487+1del | ||
NM_001136528.2:c.487+1del | ||
NM_006216.4:c.487+1del | ||
NR_073116.2:n.1148+1del |