HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208129747_208129748del , CM000664.2:g.208129747_208129748del | GRCh38 |
NC_000002.11:g.208994471_208994472del , CM000664.1:g.208994471_208994472del | GRCh37 |
NC_000002.10:g.208702716_208702717del | NCBI36 |
NG_008038.1:g.5083_5084del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282141.4:c.9+36_9+37del MANE Select | ENSP00000282141.3:n.9+36_9+37del | |
ENST00000282141.3:c.9+36_9+37del | ENSP00000282141.3:n.9+36_9+37del | |
NM_020989.3:c.9+36_9+37del | NP_066269.1:n.9+36_9+37del | |
NR_038437.1:n.98-7309_98-7308del | ||
XM_011510661.1:c.9+36_9+37del | XP_011508963.1:n.9+36_9+37del | |
XM_011510662.1:c.9+36_9+37del | XP_011508964.1:n.9+36_9+37del | |
XM_011510663.1:c.-120-65_-120-64del | XP_011508965.1:n.-120-65_-120-64del | |
NM_020989.4:c.9+36_9+37del MANE Select | NP_066269.1:n.9+36_9+37del |