HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8012137del , CM000679.2:g.8012137del | GRCh38 |
NC_000017.10:g.7915455del , CM000679.1:g.7915455del | GRCh37 |
NC_000017.9:g.7856180del | NCBI36 |
NG_009092.1:g.14468del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.1750-7del MANE Select | ENSP00000254854.4:n.1750-7del | |
ENST00000254854.4:c.1750-7del | ENSP00000254854.4:n.1750-7del | |
NM_000180.3:c.1750-7del | NP_000171.1:n.1750-7del | |
XM_011523816.1:c.1750-7del | XP_011522118.1:n.1750-7del | |
NM_000180.4:c.1750-7del MANE Select | NP_000171.1:n.1750-7del |