HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640156_640157insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.2:g.640156_640157insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | GRCh38 |
NC_000011.9:g.640156_640157insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.1:g.640156_640157insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | GRCh37 |
NC_000011.8:g.630156_630157insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | NCBI36 |
NG_021241.1:g.7852_7853insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000176183.6:c.907_908insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select | ENSP00000176183.5:p.Pro302_Pro303insArgGl... | |
ENST00000176183.5:c.907_908insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | ENSP00000176183.5:p.Pro302_Pro303insArgGl... | |
NM_000797.3:c.907_908insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | NP_000788.2:p.Pro302_Pro303insArgGlyProCy... | |
NM_000797.4:c.907_908insGGGGTCCCTGTGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select | NP_000788.2:p.Pro302_Pro303insArgGlyProCy... |