HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94111741_94111742insACT , CM000663.2:g.94111741_94111742insACT | GRCh38 |
NC_000001.10:g.94577297_94577298insACT , CM000663.1:g.94577297_94577298insACT | GRCh37 |
NC_000001.9:g.94349885_94349886insACT | NCBI36 |
NG_009073.1:g.14408_14409insAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.161-163_161-162insAGT MANE Select | ENSP00000359245.3:n.161-163_161-162insAGT | |
ENST00000649773.1:c.161-163_161-162insAGT | ENSP00000496882.1:n.161-163_161-162insAGT | |
ENST00000370225.3:c.161-163_161-162insAGT | ENSP00000359245.3:n.161-163_161-162insAGT | |
NM_000350.2:c.161-163_161-162insAGT | NP_000341.2:n.161-163_161-162insAGT | |
NM_000350.3:c.161-163_161-162insAGT MANE Select | NP_000341.2:n.161-163_161-162insAGT |