HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86647776del , CM000670.2:g.86647776del | GRCh38 |
NC_000008.10:g.87660004del , CM000670.1:g.87660004del | GRCh37 |
NC_000008.9:g.87729120del | NCBI36 |
NG_016980.1:g.100903del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.990+28del MANE Select | ENSP00000316605.5:n.990+28del | |
ENST00000681546.1:n.810+28del | ||
ENST00000681746.1:c.990+28del | ENSP00000505959.1:n.990+28del | |
ENST00000320005.5:c.990+28del | ENSP00000316605.5:n.990+28del | |
NM_019098.4:c.990+28del | NP_061971.3:n.990+28del | |
XM_011517138.1:c.576+28del | XP_011515440.1:n.576+28del | |
XM_011517138.2:c.576+28del | XP_011515440.1:n.576+28del | |
NM_019098.5:c.990+28del MANE Select | NP_061971.3:n.990+28del |