HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47335180_47335181delinsGC , CM000673.2:g.47335180_47335181delinsGC | GRCh38 |
NC_000011.9:g.47356731_47356732delinsGC , CM000673.1:g.47356731_47356732delinsGC | GRCh37 |
NC_000011.8:g.47313307_47313308delinsGC | NCBI36 |
NG_007667.1:g.22522_22523delinsGC , LRG_386:g.22522_22523delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.2766_2767delinsGC MANE Select | ENSP00000442795.1:p.Gly922= | |
ENST00000256993.8:c.2766_2767delinsGC | ENSP00000256993.5:p.Gly922= | |
ENST00000399249.6:c.2766_2767delinsGC | ENSP00000382193.2:p.Gly922= | |
ENST00000545968.5:c.2766_2767delinsGC | ENSP00000442795.1:p.Gly922= | |
NM_000256.3:c.2766_2767delinsGC , LRG_386t1:c.2766_2767delinsGC MANE Select | NP_000247.2:p.Gly922= | |
XM_011520117.1:c.2748_2749delinsGC | XP_011518419.1:p.Gly916= | |
XM_011520118.1:c.2685_2686delinsGC | XP_011518420.1:p.Gly895= |