HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990447_45990476del , CM000683.2:g.45990447_45990476del | GRCh38 |
NC_000021.8:g.47410361_47410390del , CM000683.1:g.47410361_47410390del | GRCh37 |
NC_000021.7:g.46234789_46234818del | NCBI36 |
NG_008674.1:g.13699_13728del , LRG_475:g.13699_13728del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+25_1002+54del MANE Select | ENSP00000355180.3:n.1002+25_1002+54del | |
ENST00000361866.7:c.1002+25_1002+54del | ENSP00000355180.3:n.1002+25_1002+54del | |
ENST00000612273.1:c.1002+25_1002+54del | ENSP00000483630.1:n.1002+25_1002+54del | |
NM_001848.2:c.1002+25_1002+54del , LRG_475t1:c.1002+25_1002+54del | NP_001839.2:n.1002+25_1002+54del | |
NM_001848.3:c.1002+25_1002+54del MANE Select | NP_001839.2:n.1002+25_1002+54del |