HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980510_149980511delinsTC , CM000667.2:g.149980510_149980511delinsTC | GRCh38 |
NC_000005.9:g.149360073_149360074delinsTC , CM000667.1:g.149360073_149360074delinsTC | GRCh37 |
NC_000005.8:g.149340266_149340267delinsTC | NCBI36 |
NG_007147.2:g.21628_21629delinsTC , LRG_684:g.21628_21629delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.917_918delinsTC MANE Select | ENSP00000286298.4:p.Ile306= | |
ENST00000286298.4:c.917_918delinsTC | ENSP00000286298.4:p.Ile306= | |
ENST00000503336.1:c.372+2159_372+2160delinsTC | ENSP00000426053.1:n.372+2159_372+2160delinsTC | |
NM_000112.3:c.917_918delinsTC , LRG_684t1:c.917_918delinsTC | NP_000103.2:p.Ile306= | |
XM_017009191.2:c.917_918delinsTC | XP_016864680.1:p.Ile306= | |
NM_000112.4:c.917_918delinsTC MANE Select | NP_000103.2:p.Ile306= |