HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583198_41583199insG , CM000679.2:g.41583198_41583199insG | GRCh38 |
NC_000017.10:g.39739450_39739451insG , CM000679.1:g.39739450_39739451insG | GRCh37 |
NC_000017.9:g.36992976_36992977insG | NCBI36 |
NG_008624.1:g.8697_8698insC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000167586.7:c.1274+36_1274+37insC MANE Select | ENSP00000167586.6:n.1274+36_1274+37insC | |
ENST00000167586.6:c.1274+36_1274+37insC | ENSP00000167586.6:n.1274+36_1274+37insC | |
ENST00000441550.2:n.221+36_221+37insC | ||
NM_000526.4:c.1274+36_1274+37insC | NP_000517.2:n.1274+36_1274+37insC | |
NM_000526.5:c.1274+36_1274+37insC MANE Select | NP_000517.3:n.1274+36_1274+37insC |