HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583201_41583202insC , CM000679.2:g.41583201_41583202insC | GRCh38 |
NC_000017.10:g.39739453_39739454insC , CM000679.1:g.39739453_39739454insC | GRCh37 |
NC_000017.9:g.36992979_36992980insC | NCBI36 |
NG_008624.1:g.8694_8695insG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000167586.7:c.1274+33_1274+34insG MANE Select | ENSP00000167586.6:n.1274+33_1274+34insG | |
ENST00000167586.6:c.1274+33_1274+34insG | ENSP00000167586.6:n.1274+33_1274+34insG | |
ENST00000441550.2:n.221+33_221+34insG | ||
NM_000526.4:c.1274+33_1274+34insG | NP_000517.2:n.1274+33_1274+34insG | |
NM_000526.5:c.1274+33_1274+34insG MANE Select | NP_000517.3:n.1274+33_1274+34insG |