HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443601_32443602delinsCT , CM000668.2:g.32443601_32443602delinsCT | GRCh38 |
NC_000006.11:g.32411378_32411379delinsCT , CM000668.1:g.32411378_32411379delinsCT | GRCh37 |
NC_000006.10:g.32519356_32519357delinsCT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395388.7:c.610+135_610+136delinsCT MANE Select | ENSP00000378786.2:n.610+135_610+136delinsCT | |
ENST00000374982.5:c.535+135_535+136delinsCT | ENSP00000364121.5:n.535+135_535+136delinsCT | |
ENST00000395388.6:c.610+135_610+136delinsCT | ENSP00000378786.2:n.610+135_610+136delinsCT | |
NM_019111.4:c.610+135_610+136delinsCT | NP_061984.2:n.610+135_610+136delinsCT | |
NM_019111.5:c.610+135_610+136delinsCT MANE Select | NP_061984.2:n.610+135_610+136delinsCT |