HGVS | Genome Assembly |
---|---|
NC_000005.10:g.71719676_71719677insG , CM000667.2:g.71719676_71719677insG | GRCh38 |
NC_000005.9:g.71015503_71015504insG , CM000667.1:g.71015503_71015504insG | GRCh37 |
NC_000005.8:g.71051259_71051260insG | NCBI36 |
NG_015988.1:g.5514_5515insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296777.5:c.160-204_160-203insG MANE Select | ENSP00000296777.4:n.160-204_160-203insG | |
ENST00000296777.4:c.160-204_160-203insG | ENSP00000296777.4:n.160-204_160-203insG | |
ENST00000513096.1:n.98_99insG | ||
NM_004291.3:c.160-204_160-203insG | NP_004282.1:n.160-204_160-203insG | |
NM_004291.4:c.160-204_160-203insG MANE Select | NP_004282.1:n.160-204_160-203insG |