HGVS | Genome Assembly |
---|---|
NC_000014.9:g.89568667G>A , CM000676.2:g.89568667G>A | GRCh38 |
NC_000014.8:g.90035011G>A , CM000676.1:g.90035011G>A | GRCh37 |
NC_000014.7:g.89104764G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345097.8:c.-15+50361C>T | ENSP00000343288.4:n.-15+50361C>T | |
ENST00000555353.5:c.-15+50361C>T | ENSP00000452227.1:n.-15+50361C>T | |
ENST00000555855.5:c.-118+50361C>T | ENSP00000451135.1:n.-118+50361C>T | |
NM_001085471.1:c.-15+50361C>T | NP_001078940.1:n.-15+50361C>T | |
NM_001085471.2:c.-15+50361C>T | NP_001078940.1:n.-15+50361C>T |