HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877868_6877869delinsAG , CM000670.2:g.6877868_6877869delinsAG | GRCh38 |
NC_000008.10:g.6735390_6735391delinsAG , CM000670.1:g.6735390_6735391delinsAG | GRCh37 |
NC_000008.9:g.6722800_6722801delinsAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297439.4:c.-12_-11delinsCT MANE Select | ENSP00000297439.3:n.-12_-11delinsCT | |
ENST00000297439.3:c.-12_-11delinsCT | ENSP00000297439.3:n.-12_-11delinsCT | |
NM_005218.3:c.-12_-11delinsCT | NP_005209.1:n.-12_-11delinsCT | |
NM_005218.4:c.-12_-11delinsCT MANE Select | NP_005209.1:n.-12_-11delinsCT |