HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44374994_44374998del , CM000679.2:g.44374994_44374998del | GRCh38 |
NC_000017.10:g.42452362_42452366del , CM000679.1:g.42452362_42452366del | GRCh37 |
NC_000017.9:g.39807888_39807892del | NCBI36 |
NG_008331.1:g.19514_19518del , LRG_479:g.19514_19518del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.2841+6_2841+10del | ||
ENST00000648408.1:c.2272+6_2272+10del | ||
ENST00000262407.5:c.2841+6_2841+10del | ||
ENST00000587295.5:c.253+841_253+845del | ||
ENST00000592462.5:n.2121_2125del | ||
NM_000419.3:c.2841+6_2841+10del , LRG_479t1:c.2841+6_2841+10del | ||
XM_011524749.1:c.2841+6_2841+10del | ||
XM_011524750.1:c.2841+6_2841+10del | ||
NM_000419.4:c.2841+6_2841+10del | ||
NM_000419.5:c.2841+6_2841+10del |