HGVS | Genome Assembly |
---|---|
NC_000012.12:g.114399500_114399514del , CM000674.2:g.114399500_114399514del | GRCh38 |
NC_000012.11:g.114837305_114837319del , CM000674.1:g.114837305_114837319del | GRCh37 |
NC_000012.10:g.113321688_113321702del | NCBI36 |
NG_007373.1:g.13932_13946del , LRG_670:g.13932_13946del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000405440.7:c.362+2_362+16del | ||
ENST00000310346.8:c.362+2_362+16del | ||
ENST00000349716.9:c.212+2_212+16del | ||
ENST00000405440.6:c.362+2_362+16del | ||
ENST00000526441.1:c.362+2_362+16del | ||
ENST00000552726.1:n.413+2_413+16del | ||
NM_000192.3:c.362+2_362+16del , LRG_670t1:c.362+2_362+16del | ||
NM_080717.2:c.212+2_212+16del | ||
NM_181486.2:c.362+2_362+16del | ||
XM_017019912.1:c.410+2_410+16del | ||
NM_080717.3:c.212+2_212+16del | ||
NM_181486.4:c.362+2_362+16del | ||
NM_080717.4:c.212+2_212+16del |