HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42544241_42544242del , CM000679.2:g.42544241_42544242del | GRCh38 |
NC_000017.10:g.40696259_40696260del , CM000679.1:g.40696259_40696260del | GRCh37 |
NC_000017.9:g.37949785_37949786del | NCBI36 |
NG_011552.1:g.13309_13310del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.*3_*4del MANE Select | ENSP00000225927.1:n.*3_*4del | |
ENST00000225927.6:c.*3_*4del | ENSP00000225927.1:n.*3_*4del | |
NM_000263.3:c.*3_*4del | NP_000254.2:n.*3_*4del | |
XM_006721920.2:c.*3_*4del | XP_006721983.1:n.*3_*4del | |
XM_011524840.1:c.*3_*4del | XP_011523142.1:n.*3_*4del | |
XM_017024687.1:c.*3_*4del | XP_016880176.1:n.*3_*4del | |
XM_024450771.1:c.*3_*4del | XP_024306539.1:n.*3_*4del | |
XM_024450772.1:c.*3_*4del | XP_024306540.1:n.*3_*4del | |
NM_000263.4:c.*3_*4del MANE Select | NP_000254.2:n.*3_*4del |