HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31357579_31357598del , CM000668.2:g.31357579_31357598del | GRCh38 |
NC_000006.11:g.31325356_31325375del , CM000668.1:g.31325356_31325375del | GRCh37 |
NC_000006.10:g.31433335_31433354del | NCBI36 |
NG_023187.1:g.4621_4640del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000474381.2:n.1338+22_1338+41del | ||
ENST00000481849.6:n.1338+22_1338+41del | ||
ENST00000497377.6:n.1338+22_1338+41del | ||
ENST00000696559.1:c.-136+22_-136+41del | ENSP00000512717.1:n.-136+22_-136+41del | |
ENST00000696560.1:c.-136+22_-136+41del | ENSP00000512718.1:n.-136+22_-136+41del | |
ENST00000696561.1:c.-136+22_-136+41del | ENSP00000512719.1:n.-136+22_-136+41del | |
ENST00000696562.1:c.-135-299_-135-280del | ENSP00000512720.1:n.-135-299_-135-280del | |
ENST00000603274.1:n.933_952del | ||
XR_926692.1:n.164+22_164+41del |