HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43886945_43886946insC , CM000664.2:g.43886945_43886946insC | GRCh38 |
NC_000002.11:g.44114084_44114085insC , CM000664.1:g.44114084_44114085insC | GRCh37 |
NC_000002.10:g.43967588_43967589insC | NCBI36 |
NG_008247.1:g.114060_114061insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682612.1:c.2606_2607insG | ||
ENST00000684454.1:n.9703_9704insG | ||
ENST00000260665.12:c.*1654_*1655insG MANE Select | ENSP00000260665.7:n.*1654_*1655insG | |
ENST00000260665.11:c.*1654_*1655insG | ENSP00000260665.7:n.*1654_*1655insG | |
NM_133259.3:c.*1654_*1655insG | NP_573566.2:n.*1654_*1655insG | |
XR_002958896.1:n.6021_6022insG | ||
NM_133259.4:c.*1654_*1655insG MANE Select | NP_573566.2:n.*1654_*1655insG |