HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177994326_177994338del , CM000667.2:g.177994326_177994338del | GRCh38 |
NC_000005.9:g.177421327_177421339del , CM000667.1:g.177421327_177421339del | GRCh37 |
NC_000005.8:g.177353933_177353945del | NCBI36 |
NG_015889.1:g.6907_6919del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000308304.2:c.112_124del MANE Select | ENSP00000311290.2:p.Ser38ProfsTer? | |
NM_006261.4:c.112_124del | NP_006252.3:p.Ser38ProfsTer? | |
NM_006261.5:c.112_124del MANE Select | NP_006252.4:p.Ser38ProfsTer? |