HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990481_45990482insTG , CM000683.2:g.45990481_45990482insTG | GRCh38 |
NC_000021.8:g.47410395_47410396insTG , CM000683.1:g.47410395_47410396insTG | GRCh37 |
NC_000021.7:g.46234823_46234824insTG | NCBI36 |
NG_008674.1:g.13733_13734insTG , LRG_475:g.13733_13734insTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+59_1002+60insTG MANE Select | ENSP00000355180.3:n.1002+59_1002+60insTG | |
ENST00000361866.7:c.1002+59_1002+60insTG | ENSP00000355180.3:n.1002+59_1002+60insTG | |
ENST00000612273.1:c.1002+59_1002+60insTG | ENSP00000483630.1:n.1002+59_1002+60insTG | |
NM_001848.2:c.1002+59_1002+60insTG , LRG_475t1:c.1002+59_1002+60insTG | NP_001839.2:n.1002+59_1002+60insTG | |
NM_001848.3:c.1002+59_1002+60insTG MANE Select | NP_001839.2:n.1002+59_1002+60insTG |