HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990450_45990498del , CM000683.2:g.45990450_45990498del | GRCh38 |
NC_000021.8:g.47410364_47410412del , CM000683.1:g.47410364_47410412del | GRCh37 |
NC_000021.7:g.46234792_46234840del | NCBI36 |
NG_008674.1:g.13702_13750del , LRG_475:g.13702_13750del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+28_1002+76del MANE Select | ENSP00000355180.3:n.1002+28_1002+76del | |
ENST00000361866.7:c.1002+28_1002+76del | ENSP00000355180.3:n.1002+28_1002+76del | |
ENST00000612273.1:c.1002+28_1002+76del | ENSP00000483630.1:n.1002+28_1002+76del | |
NM_001848.2:c.1002+28_1002+76del , LRG_475t1:c.1002+28_1002+76del | NP_001839.2:n.1002+28_1002+76del | |
NM_001848.3:c.1002+28_1002+76del MANE Select | NP_001839.2:n.1002+28_1002+76del |