HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152307666_152307667insG , CM000663.2:g.152307666_152307667insG | GRCh38 |
NC_000001.10:g.152280142_152280143insG , CM000663.1:g.152280142_152280143insG | GRCh37 |
NC_000001.9:g.150546766_150546767insG | NCBI36 |
NG_016190.1:g.22537_22538insC , LRG_1028:g.22537_22538insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.7219_7220insC MANE Select | ENSP00000357789.1:p.Arg2407ThrfsTer16 | |
ENST00000368799.1:c.7219_7220insC | ENSP00000357789.1:p.Arg2407ThrfsTer16 | |
NM_002016.1:c.7219_7220insC , LRG_1028t1:c.7219_7220insC | NP_002007.1:p.Arg2407ThrfsTer16 | |
XM_011509329.1:c.7219_7220insC | XP_011507631.1:p.Arg2407ThrfsTer16 | |
NM_002016.2:c.7219_7220insC MANE Select | NP_002007.1:p.Arg2407ThrfsTer16 |