HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443666_33443667insC , CM000682.2:g.33443666_33443667insC | GRCh38 |
NC_000020.10:g.32031472_32031473insC , CM000682.1:g.32031472_32031473insC | GRCh37 |
NC_000020.9:g.31495133_31495134insC | NCBI36 |
NG_011622.1:g.5226_5227insG , LRG_332:g.5226_5227insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.-47_-46insG MANE Select | ENSP00000217381.2:n.-47_-46insG | |
ENST00000217381.2:c.-47_-46insG | ENSP00000217381.2:n.-47_-46insG | |
NM_003098.2:c.-47_-46insG , LRG_332t1:c.-47_-46insG | NP_003089.1:n.-47_-46insG | |
XM_005260517.1:c.-47_-46insG | XP_005260574.1:n.-47_-46insG | |
XM_011529007.1:c.-47_-46insG | XP_011527309.1:n.-47_-46insG | |
XM_011529008.1:c.-47_-46insG | XP_011527310.1:n.-47_-46insG | |
XR_936612.1:n.187_188insG | ||
NM_003098.3:c.-47_-46insG MANE Select | NP_003089.1:n.-47_-46insG |