HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640156_640157insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.2:g.640156_640157insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | GRCh38 |
NC_000011.9:g.640156_640157insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC , CM000673.1:g.640156_640157insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | GRCh37 |
NC_000011.8:g.630156_630157insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | NCBI36 |
NG_021241.1:g.7852_7853insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000176183.6:c.907_908insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select | ENSP00000176183.5:p.Pro302_Pro303insGlnAs... | |
ENST00000176183.5:c.907_908insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | ENSP00000176183.5:p.Pro302_Pro303insGlnAs... | |
NM_000797.3:c.907_908insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC | NP_000788.2:p.Pro302_Pro303insGlnAspProCy... | |
NM_000797.4:c.907_908insAGGACCCCTGCGGCTCCAACTGTGCGCCCCCCGCGCCCGGCCTCCCCC MANE Select | NP_000788.2:p.Pro302_Pro303insGlnAspProCy... |