HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73329567_73329568del , CM000677.2:g.73329567_73329568del | GRCh38 |
NC_000015.9:g.73621908_73621909del , CM000677.1:g.73621908_73621909del | GRCh37 |
NC_000015.8:g.71408961_71408962del | NCBI36 |
NG_009063.1:g.44697_44698del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.1590+5_1590+6del MANE Select | ENSP00000261917.3:n.1590+5_1590+6del | |
ENST00000261917.3:c.1590+5_1590+6del | ENSP00000261917.3:n.1590+5_1590+6del | |
NM_005477.2:c.1590+5_1590+6del | NP_005468.1:n.1590+5_1590+6del | |
XM_011521148.1:c.372+5_372+6del | XP_011519450.1:n.372+5_372+6del | |
XM_011521148.2:c.372+5_372+6del | XP_011519450.1:n.372+5_372+6del | |
NM_005477.3:c.1590+5_1590+6del MANE Select | NP_005468.1:n.1590+5_1590+6del |