HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204165224_204165225delinsGC , CM000663.2:g.204165224_204165225delinsGC | GRCh38 |
NC_000001.10:g.204134352_204134353delinsGC , CM000663.1:g.204134352_204134353delinsGC | GRCh37 |
NC_000001.9:g.202400975_202400976delinsGC | NCBI36 |
NG_012122.1:g.6113_6114delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272190.9:c.98+971_98+972delinsGC MANE Select | ENSP00000272190.8:n.98+971_98+972delinsGC | |
ENST00000638118.1:c.-16-3062_-16-3061delinsGC | ENSP00000490307.1:n.-16-3062_-16-3061delinsGC | |
ENST00000272190.8:c.98+971_98+972delinsGC | ENSP00000272190.8:n.98+971_98+972delinsGC | |
NM_000537.3:c.98+971_98+972delinsGC | NP_000528.1:n.98+971_98+972delinsGC | |
NM_000537.4:c.98+971_98+972delinsGC MANE Select | NP_000528.1:n.98+971_98+972delinsGC |