HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980269_149980272del , CM000667.2:g.149980269_149980272del | GRCh38 |
NC_000005.9:g.149359832_149359835del , CM000667.1:g.149359832_149359835del | GRCh37 |
NC_000005.8:g.149340025_149340028del | NCBI36 |
NG_007147.2:g.21387_21390del , LRG_684:g.21387_21390del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.700-24_700-21del MANE Select | ENSP00000286298.4:n.700-24_700-21del | |
ENST00000286298.4:c.700-24_700-21del | ENSP00000286298.4:n.700-24_700-21del | |
ENST00000503336.1:c.372+1918_372+1921del | ENSP00000426053.1:n.372+1918_372+1921del | |
NM_000112.3:c.700-24_700-21del , LRG_684t1:c.700-24_700-21del | NP_000103.2:n.700-24_700-21del | |
XM_017009191.2:c.700-24_700-21del | XP_016864680.1:n.700-24_700-21del | |
NM_000112.4:c.700-24_700-21del MANE Select | NP_000103.2:n.700-24_700-21del |