HGVS | Genome Assembly |
---|---|
NC_000002.12:g.111947553_111947570del , CM000664.2:g.111947553_111947570del | GRCh38 |
NC_000002.11:g.112705130_112705147del , CM000664.1:g.112705130_112705147del | GRCh37 |
NC_000002.10:g.112421601_112421618del | NCBI36 |
NG_011607.1:g.53940_53957del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295408.9:c.743_757+3del | ||
ENST00000295408.8:c.743_757+3del | ||
ENST00000409780.5:c.215_229+3del | ||
ENST00000421804.6:c.743_757+3del | ||
ENST00000439966.5:c.*216_*230+3del | ||
ENST00000616902.4:c.-473_-459+3del | ||
NM_006343.2:c.743_757+3del | ||
XM_005263565.3:c.743_757+3del | ||
XM_005263568.3:c.743_757+3del | ||
XM_011510490.1:c.554_568+3del | ||
XM_005263565.4:c.743_757+3del | ||
XM_005263568.4:c.743_757+3del | ||
XM_011510490.3:c.554_568+3del | ||
XM_017003164.1:c.554_568+3del | ||
XM_017003165.2:c.-525_-511+3del | ||
NM_006343.3:c.743_757+3del |