HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443576_32443577insAG , CM000668.2:g.32443576_32443577insAG | GRCh38 |
NC_000006.11:g.32411353_32411354insAG , CM000668.1:g.32411353_32411354insAG | GRCh37 |
NC_000006.10:g.32519331_32519332insAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.610+110_610+111insAG MANE Select | ENSP00000378786.2:n.610+110_610+111insAG | |
ENST00000374982.5:c.535+110_535+111insAG | ENSP00000364121.5:n.535+110_535+111insAG | |
ENST00000395388.6:c.610+110_610+111insAG | ENSP00000378786.2:n.610+110_610+111insAG | |
NM_019111.4:c.610+110_610+111insAG | NP_061984.2:n.610+110_610+111insAG | |
NM_019111.5:c.610+110_610+111insAG MANE Select | NP_061984.2:n.610+110_610+111insAG |