HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583712_41583713insTT , CM000679.2:g.41583712_41583713insTT | GRCh38 |
NC_000017.10:g.39739964_39739965insTT , CM000679.1:g.39739964_39739965insTT | GRCh37 |
NC_000017.9:g.36993490_36993491insTT | NCBI36 |
NG_008624.1:g.8183_8184insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.928-37_928-36insAA MANE Select | ENSP00000167586.6:n.928-37_928-36insAA | |
ENST00000167586.6:c.928-37_928-36insAA | ENSP00000167586.6:n.928-37_928-36insAA | |
ENST00000476662.1:n.378-37_378-36insAA | ||
NM_000526.4:c.928-37_928-36insAA | NP_000517.2:n.928-37_928-36insAA | |
NM_000526.5:c.928-37_928-36insAA MANE Select | NP_000517.3:n.928-37_928-36insAA |