HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160127636_160127637delinsAA , CM000663.2:g.160127636_160127637delinsAA | GRCh38 |
NC_000001.10:g.160097426_160097427delinsAA , CM000663.1:g.160097426_160097427delinsAA | GRCh37 |
NC_000001.9:g.158364050_158364051delinsAA | NCBI36 |
NG_008014.1:g.16879_16880delinsAA , LRG_6:g.16879_16880delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.833_834delinsAA MANE Select | ENSP00000354490.3:p.Gly278Glu | |
ENST00000361216.7:c.833_834delinsAA | ENSP00000354490.3:p.Gly278Glu | |
ENST00000392233.7:c.833_834delinsAA | ENSP00000376066.3:p.Gly278Glu | |
ENST00000472488.5:n.936_937delinsAA | ||
NM_000702.3:c.833_834delinsAA | NP_000693.1:p.Gly278Glu | |
NM_000702.4:c.833_834delinsAA MANE Select | NP_000693.1:p.Gly278Glu |