HGVS | Genome Assembly |
---|---|
NC_000015.10:g.39581165del , CM000677.2:g.39581165del | GRCh38 |
NC_000015.9:g.39873366del , CM000677.1:g.39873366del | GRCh37 |
NC_000015.8:g.37660658del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260356.6:c.-93del MANE Select | ENSP00000260356.5:n.-93del | |
ENST00000260356.5:c.-93del | ENSP00000260356.5:n.-93del | |
ENST00000397591.2:c.-214del | ENSP00000380720.2:n.-214del | |
NM_003246.2:c.-93del | NP_003237.2:n.-93del | |
NM_003246.3:c.-93del | NP_003237.2:n.-93del | |
XM_011521970.1:c.-214del | XP_011520272.1:n.-214del | |
XM_011521971.1:c.-93del | XP_011520273.1:n.-93del | |
XR_931897.1:n.83del | ||
XM_011521971.2:c.-93del | XP_011520273.1:n.-93del | |
NM_003246.4:c.-93del MANE Select | NP_003237.2:n.-93del |