HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45461844_45461845delinsAC , CM000667.2:g.45461844_45461845delinsAC | GRCh38 |
NC_000005.9:g.45461946_45461947delinsAC , CM000667.1:g.45461946_45461947delinsAC | GRCh37 |
NC_000005.8:g.45497703_45497704delinsAC | NCBI36 |
NG_042183.1:g.239274_239275delinsGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303230.6:c.1011+1_1011+2delinsGT MANE Select | ENSP00000307342.4:n.1011+1_1011+2delinsGT... | |
ENST00000637305.1:n.174+1_174+2delinsGT | ||
ENST00000673735.1:c.1011+1_1011+2delinsGT | ENSP00000501107.1:n.1011+1_1011+2delinsGT... | |
ENST00000303230.5:c.1011+1_1011+2delinsGT | ENSP00000307342.4:n.1011+1_1011+2delinsGT... | |
NM_021072.3:c.1011+1_1011+2delinsGT | NP_066550.2:n.1011+1_1011+2delinsGT | |
NM_021072.4:c.1011+1_1011+2delinsGT MANE Select | NP_066550.2:n.1011+1_1011+2delinsGT |