HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145547_38145548del , CM000670.2:g.38145547_38145548del | GRCh38 |
NC_000008.10:g.38003065_38003066del , CM000670.1:g.38003065_38003066del | GRCh37 |
NC_000008.9:g.38122222_38122223del | NCBI36 |
NG_011827.1:g.10535_10536del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.651-233_651-232del MANE Select | ENSP00000276449.3:n.651-233_651-232del | |
ENST00000276449.8:c.651-233_651-232del | ENSP00000276449.3:n.651-233_651-232del | |
ENST00000520114.1:n.1552_1553del | ||
ENST00000522050.1:c.586+415_586+416del | ||
NM_000349.2:c.651-233_651-232del | NP_000340.2:n.651-233_651-232del | |
XM_006716392.1:c.650+415_650+416del | XP_006716455.1:n.650+415_650+416del | |
NM_000349.3:c.651-233_651-232del MANE Select | NP_000340.2:n.651-233_651-232del |