HGVS | Genome Assembly |
---|---|
NC_000010.11:g.86917134del , CM000672.2:g.86917134del | GRCh38 |
NC_000010.10:g.88676891del , CM000672.1:g.88676891del | GRCh37 |
NC_000010.9:g.88666871del | NCBI36 |
NG_009362.1:g.165496del , LRG_298:g.165496del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000480152.3:c.676del | ||
ENST00000635816.2:c.676del | ||
ENST00000636056.2:c.676del | ||
ENST00000372037.8:c.676del | ||
ENST00000635816.1:c.676del | ||
ENST00000636056.1:c.676del | ||
ENST00000638429.1:c.676del | ||
ENST00000372037.7:c.676del | ||
NM_004329.2:c.676del , LRG_298t1:c.676del | ||
XM_011540103.1:c.676del | ||
XM_011540104.1:c.676del | ||
XM_011540103.2:c.676del | ||
XM_011540104.2:c.676del | ||
NM_004329.3:c.676del |