HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50459712_50459713del , CM000685.2:g.50459712_50459713del | GRCh38 |
NC_000023.10:g.50202710_50202711del , CM000685.1:g.50202710_50202711del | GRCh37 |
NC_000023.9:g.50219450_50219451del | NCBI36 |
NG_033143.2:g.16010_16011del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000611977.2:c.645+10321_645+10322del MANE Select | ENSP00000477515.1:n.645+10321_645+10322del | |
ENST00000611977.1:c.645+10321_645+10322del | ENSP00000477515.1:n.645+10321_645+10322del | |
NM_001013742.3:c.645+10321_645+10322del | NP_001013764.1:n.645+10321_645+10322del | |
XM_017029268.2:c.645+10321_645+10322del | XP_016884757.1:n.645+10321_645+10322del | |
NM_001013742.4:c.645+10321_645+10322del MANE Select | NP_001013764.1:n.645+10321_645+10322del |