HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5045051_5045052delinsGG , CM000674.2:g.5045051_5045052delinsGG | GRCh38 |
NC_000012.11:g.5154217_5154218delinsGG , CM000674.1:g.5154217_5154218delinsGG | GRCh37 |
NC_000012.10:g.5024478_5024479delinsGG | NCBI36 |
NG_012198.1:g.6133_6134delinsGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.904_905delinsGG MANE Select | ENSP00000252321.3:p.Gly302= | |
ENST00000252321.4:c.904_905delinsGG | ENSP00000252321.3:p.Gly302= | |
NM_002234.3:c.904_905delinsGG | NP_002225.2:p.Gly302= | |
NM_002234.4:c.904_905delinsGG MANE Select | NP_002225.2:p.Gly302= |