HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990462_45990463insC , CM000683.2:g.45990462_45990463insC | GRCh38 |
NC_000021.8:g.47410376_47410377insC , CM000683.1:g.47410376_47410377insC | GRCh37 |
NC_000021.7:g.46234804_46234805insC | NCBI36 |
NG_008674.1:g.13714_13715insC , LRG_475:g.13714_13715insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+40_1002+41insC MANE Select | ENSP00000355180.3:n.1002+40_1002+41insC | |
ENST00000361866.7:c.1002+40_1002+41insC | ENSP00000355180.3:n.1002+40_1002+41insC | |
ENST00000612273.1:c.1002+40_1002+41insC | ENSP00000483630.1:n.1002+40_1002+41insC | |
NM_001848.2:c.1002+40_1002+41insC , LRG_475t1:c.1002+40_1002+41insC | NP_001839.2:n.1002+40_1002+41insC | |
NM_001848.3:c.1002+40_1002+41insC MANE Select | NP_001839.2:n.1002+40_1002+41insC |