HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443838_32443839insGAG , CM000668.2:g.32443838_32443839insGAG | GRCh38 |
NC_000006.11:g.32411615_32411616insGAG , CM000668.1:g.32411615_32411616insGAG | GRCh37 |
NC_000006.10:g.32519593_32519594insGAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.693_694insGAG MANE Select | ENSP00000378786.2:p.Ile231_Ile232insGlu | |
ENST00000374982.5:c.618_619insGAG | ENSP00000364121.5:p.Ile206_Ile207insGlu | |
ENST00000395388.6:c.693_694insGAG | ENSP00000378786.2:p.Ile231_Ile232insGlu | |
NM_019111.4:c.693_694insGAG | NP_061984.2:p.Ile231_Ile232insGlu | |
NM_019111.5:c.693_694insGAG MANE Select | NP_061984.2:p.Ile231_Ile232insGlu |