HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23433559_23433560insCC , CM000676.2:g.23433559_23433560insCC | GRCh38 |
NC_000014.8:g.23902768_23902769insCC , CM000676.1:g.23902768_23902769insCC | GRCh37 |
NC_000014.7:g.22972608_22972609insCC | NCBI36 |
NG_007884.1:g.7102_7103insGG , LRG_384:g.7102_7103insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.173_174insGG MANE Select | ENSP00000347507.3:p.Val59GlufsTer12 | |
ENST00000355349.3:c.173_174insGG | ENSP00000347507.3:p.Val59GlufsTer12 | |
NM_000257.3:c.173_174insGG | NP_000248.2:p.Val59GlufsTer12 | |
XR_245686.3:n.279_280insGG | ||
XM_017021340.1:c.173_174insGG | XP_016876829.1:p.Val59GlufsTer12 | |
NM_000257.4:c.173_174insGG MANE Select | NP_000248.2:p.Val59GlufsTer12 |