HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40843715_40843716insAC , CM000681.2:g.40843715_40843716insAC | GRCh38 |
NC_000019.9:g.41349620_41349621insAC , CM000681.1:g.41349620_41349621insAC | GRCh37 |
NC_000019.8:g.46041460_46041461insAC | NCBI36 |
NG_008377.1:g.11732_11733insGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301141.10:c.*80_*81insGT MANE Select | ENSP00000301141.4:n.*80_*81insGT | |
ENST00000301141.9:c.*80_*81insGT | ENSP00000301141.4:n.*80_*81insGT | |
ENST00000599960.1:n.484_485insGT | ||
ENST00000601627.1:c.119+42300_119+42301insAC | ||
NM_000762.5:c.*80_*81insGT | NP_000753.3:n.*80_*81insGT | |
NM_000762.6:c.*80_*81insGT MANE Select | NP_000753.3:n.*80_*81insGT |