HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990478_45990479insACCG , CM000683.2:g.45990478_45990479insACCG | GRCh38 |
NC_000021.8:g.47410392_47410393insACCG , CM000683.1:g.47410392_47410393insACCG | GRCh37 |
NC_000021.7:g.46234820_46234821insACCG | NCBI36 |
NG_008674.1:g.13730_13731insACCG , LRG_475:g.13730_13731insACCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+56_1002+57insACCG MANE Select | ENSP00000355180.3:n.1002+56_1002+57insACCG | |
ENST00000361866.7:c.1002+56_1002+57insACCG | ENSP00000355180.3:n.1002+56_1002+57insACCG | |
ENST00000612273.1:c.1002+56_1002+57insACCG | ENSP00000483630.1:n.1002+56_1002+57insACCG | |
NM_001848.2:c.1002+56_1002+57insACCG , LRG_475t1:c.1002+56_1002+57insACCG | NP_001839.2:n.1002+56_1002+57insACCG | |
NM_001848.3:c.1002+56_1002+57insACCG MANE Select | NP_001839.2:n.1002+56_1002+57insACCG |