HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145861_38145865del , CM000670.2:g.38145861_38145865del | GRCh38 |
NC_000008.10:g.38003379_38003383del , CM000670.1:g.38003379_38003383del | GRCh37 |
NC_000008.9:g.38122536_38122540del | NCBI36 |
NG_011827.1:g.10218_10222del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.650+98_650+102del MANE Select | ENSP00000276449.3:n.650+98_650+102del | |
ENST00000276449.8:c.650+98_650+102del | ENSP00000276449.3:n.650+98_650+102del | |
ENST00000520114.1:n.1235_1239del | ||
ENST00000522050.1:c.586+98_586+102del | ||
NM_000349.2:c.650+98_650+102del | NP_000340.2:n.650+98_650+102del | |
XM_006716392.1:c.650+98_650+102del | XP_006716455.1:n.650+98_650+102del | |
NM_000349.3:c.650+98_650+102del MANE Select | NP_000340.2:n.650+98_650+102del |