HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610382_1610425del , CM000668.2:g.1610382_1610425del | GRCh38 |
NC_000006.11:g.1610617_1610660del , CM000668.1:g.1610617_1610660del | GRCh37 |
NC_000006.10:g.1555616_1555659del | NCBI36 |
NG_009368.1:g.4937_4980del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645831.2:c.-64_-21del MANE Select | ENSP00000493906.1:n.-64_-21del | |
ENST00000380874.3:c.-64_-21del | ENSP00000370256.2:n.-64_-21del | |
NM_001453.3:c.-64_-21del MANE Select | NP_001444.2:n.-64_-21del |