HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177993199_177993200insACT , CM000667.2:g.177993199_177993200insACT | GRCh38 |
NC_000005.9:g.177420200_177420201insACT , CM000667.1:g.177420200_177420201insACT | GRCh37 |
NC_000005.8:g.177352806_177352807insACT | NCBI36 |
NG_015889.1:g.8043_8044insAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.343-153_343-152insAGT MANE Select | ENSP00000311290.2:n.343-153_343-152insAGT | |
NM_006261.4:c.343-153_343-152insAGT | NP_006252.3:n.343-153_343-152insAGT | |
NM_006261.5:c.343-153_343-152insAGT MANE Select | NP_006252.4:n.343-153_343-152insAGT |