HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94030952_94030953delinsGC , CM000663.2:g.94030952_94030953delinsGC | GRCh38 |
NC_000001.10:g.94496508_94496509delinsGC , CM000663.1:g.94496508_94496509delinsGC | GRCh37 |
NC_000001.9:g.94269096_94269097delinsGC | NCBI36 |
NG_009073.1:g.95197_95198delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.4253+43_4253+44delinsGC MANE Select | ENSP00000359245.3:n.4253+43_4253+44delins... | |
ENST00000370225.3:c.4253+43_4253+44delinsGC | ENSP00000359245.3:n.4253+43_4253+44delins... | |
ENST00000536513.5:c.629+43_629+44delinsGC | ENSP00000439707.2:n.629+43_629+44delinsGC... | |
NM_000350.2:c.4253+43_4253+44delinsGC | NP_000341.2:n.4253+43_4253+44delinsGC | |
NM_000350.3:c.4253+43_4253+44delinsGC MANE Select | NP_000341.2:n.4253+43_4253+44delinsGC |