HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367857_73367858insC , CM000677.2:g.73367857_73367858insC | GRCh38 |
NC_000015.9:g.73660198_73660199insC , CM000677.1:g.73660198_73660199insC | GRCh37 |
NC_000015.8:g.71447251_71447252insC | NCBI36 |
NG_009063.1:g.6407_6408insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.413_414insG MANE Select | ENSP00000261917.3:p.Gly140ArgfsTer? | |
ENST00000261917.3:c.413_414insG | ENSP00000261917.3:p.Gly140ArgfsTer? | |
NM_005477.2:c.413_414insG | NP_005468.1:p.Gly140ArgfsTer? | |
NM_005477.3:c.413_414insG MANE Select | NP_005468.1:p.Gly140ArgfsTer? |