HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102842595_102842597del , CM000673.2:g.102842595_102842597del | GRCh38 |
NC_000011.9:g.102713326_102713328del , CM000673.1:g.102713326_102713328del | GRCh37 |
NC_000011.8:g.102218536_102218538del | NCBI36 |
NG_012100.1:g.6015_6017del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299855.10:c.351-18_351-16del MANE Select | ENSP00000299855.5:n.351-18_351-16del | |
ENST00000299855.9:c.351-18_351-16del | ENSP00000299855.5:n.351-18_351-16del | |
ENST00000524478.1:c.*193-18_*193-16del | ENSP00000435255.1:n.*193-18_*193-16del | |
NM_002422.3:c.351-18_351-16del | NP_002413.1:n.351-18_351-16del | |
NM_002422.4:c.351-18_351-16del | NP_002413.1:n.351-18_351-16del | |
NM_002422.5:c.351-18_351-16del MANE Select | NP_002413.1:n.351-18_351-16del |