HGVS | Genome Assembly |
---|---|
NC_000017.11:g.50199329_50199418del , CM000679.2:g.50199329_50199418del | GRCh38 |
NC_000017.10:g.48276690_48276779del , CM000679.1:g.48276690_48276779del | GRCh37 |
NC_000017.9:g.45631689_45631778del | NCBI36 |
NG_007400.1:g.7224_7313del , LRG_1:g.7224_7313del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000225964.10:c.369+2_370del | ||
ENST00000225964.9:c.369+2_370del | ||
ENST00000474644.1:n.590+2_591del | ||
ENST00000507689.1:c.423+2_424del | ||
NM_000088.3:c.369+2_370del , LRG_1t1:c.369+2_370del | ||
XM_005257058.3:c.369+2_370del | ||
XM_005257059.3:c.369+2_370del | ||
XM_011524341.1:c.369+2_370del | ||
XM_005257058.4:c.369+2_370del | ||
XM_005257059.4:c.369+2_370del | ||
NM_000088.4:c.369+2_370del |