HGVS | Genome Assembly |
---|---|
NC_000018.10:g.59269140_59269141insC , CM000680.2:g.59269140_59269141insC | GRCh38 |
NC_000018.9:g.56936372_56936373insC , CM000680.1:g.56936372_56936373insC | GRCh37 |
NC_000018.8:g.55087352_55087353insC | NCBI36 |
NG_013031.1:g.9253_9254insG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000334889.4:c.904_905insG MANE Select | ENSP00000334813.3:p.Ser302CysfsTer? | |
ENST00000256852.7:c.*335_*336insG | ENSP00000256852.7:n.*335_*336insG | |
ENST00000334889.3:c.904_905insG | ENSP00000334813.3:p.Ser302CysfsTer? | |
NM_013435.2:c.904_905insG | NP_038463.2:p.Ser302CysfsTer? | |
NM_013435.3:c.904_905insG MANE Select | NP_038463.2:p.Ser302CysfsTer? |