HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714015_114714016insC , CM000663.2:g.114714015_114714016insC | GRCh38 |
NC_000001.10:g.115256636_115256637insC , CM000663.1:g.115256636_115256637insC | GRCh37 |
NC_000001.9:g.115058159_115058160insC | NCBI36 |
NG_007572.1:g.7879_7880insG , LRG_92:g.7879_7880insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-38_112-37insG MANE Select | ENSP00000358548.4:n.112-38_112-37insG | |
ENST00000369535.4:c.112-38_112-37insG | ENSP00000358548.4:n.112-38_112-37insG | |
NM_002524.4:c.112-38_112-37insG | NP_002515.1:n.112-38_112-37insG | |
NM_002524.5:c.112-38_112-37insG MANE Select | NP_002515.1:n.112-38_112-37insG |