HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990611_45990612dup , CM000683.2:g.45990611_45990612dup | GRCh38 |
NC_000021.8:g.47410525_47410526dup , CM000683.1:g.47410525_47410526dup | GRCh37 |
NC_000021.7:g.46234953_46234954dup | NCBI36 |
NG_008674.1:g.13863_13864dup , LRG_475:g.13863_13864dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1003-162_1003-161dup MANE Select | ENSP00000355180.3:n.1003-162_1003-161dup | |
ENST00000361866.7:c.1003-162_1003-161dup | ENSP00000355180.3:n.1003-162_1003-161dup | |
ENST00000612273.1:c.1003-162_1003-161dup | ENSP00000483630.1:n.1003-162_1003-161dup | |
NM_001848.2:c.1003-162_1003-161dup , LRG_475t1:c.1003-162_1003-161dup | NP_001839.2:n.1003-162_1003-161dup | |
NM_001848.3:c.1003-162_1003-161dup MANE Select | NP_001839.2:n.1003-162_1003-161dup |