HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46859476del , CM000665.2:g.46859476del | GRCh38 |
NC_000003.11:g.46900966del , CM000665.1:g.46900966del | GRCh37 |
NC_000003.10:g.46875970del | NCBI36 |
NG_007555.2:g.27696del , LRG_395:g.27696del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000431168.2:c.481+1del | ||
ENST00000292327.6:c.481+1del | ||
ENST00000653454.1:c.481+1del | ||
ENST00000654597.1:c.481+1del | ||
ENST00000655244.1:n.703+1del | ||
ENST00000662933.1:c.481+1del | ||
ENST00000664891.1:n.439+1del | ||
ENST00000292327.4:c.481+1del | ||
ENST00000395869.5:c.481+1del | ||
NM_000258.2:c.481+1del , LRG_395t1:c.481+1del | ||
NM_000258.3:c.481+1del |