HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990517_45990518insC , CM000683.2:g.45990517_45990518insC | GRCh38 |
NC_000021.8:g.47410431_47410432insC , CM000683.1:g.47410431_47410432insC | GRCh37 |
NC_000021.7:g.46234859_46234860insC | NCBI36 |
NG_008674.1:g.13769_13770insC , LRG_475:g.13769_13770insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+95_1002+96insC MANE Select | ENSP00000355180.3:n.1002+95_1002+96insC | |
ENST00000361866.7:c.1002+95_1002+96insC | ENSP00000355180.3:n.1002+95_1002+96insC | |
ENST00000612273.1:c.1002+95_1002+96insC | ENSP00000483630.1:n.1002+95_1002+96insC | |
NM_001848.2:c.1002+95_1002+96insC , LRG_475t1:c.1002+95_1002+96insC | NP_001839.2:n.1002+95_1002+96insC | |
NM_001848.3:c.1002+95_1002+96insC MANE Select | NP_001839.2:n.1002+95_1002+96insC |