HGVS | Genome Assembly |
---|---|
NC_000020.11:g.38363455_38363456delinsAG , CM000682.2:g.38363455_38363456delinsAG | GRCh38 |
NC_000020.10:g.36992109_36992110delinsAG , CM000682.1:g.36992109_36992110delinsAG | GRCh37 |
NC_000020.9:g.36425523_36425524delinsAG | NCBI36 |
NG_034239.1:g.22045_22046delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217407.3:c.653-520_653-519delinsAG MANE Select | ENSP00000217407.2:n.653-520_653-519delinsAG | |
ENST00000217407.2:c.653-520_653-519delinsAG | ENSP00000217407.2:n.653-520_653-519delinsAG | |
NM_004139.4:c.653-520_653-519delinsAG | NP_004130.2:n.653-520_653-519delinsAG | |
NM_004139.5:c.653-520_653-519delinsAG MANE Select | NP_004130.2:n.653-520_653-519delinsAG |