HGVS | Genome Assembly |
---|---|
NC_000014.9:g.89568722C>T , CM000676.2:g.89568722C>T | GRCh38 |
NC_000014.8:g.90035066C>T , CM000676.1:g.90035066C>T | GRCh37 |
NC_000014.7:g.89104819C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345097.8:c.-15+50306G>A | ENSP00000343288.4:n.-15+50306G>A | |
ENST00000555353.5:c.-15+50306G>A | ENSP00000452227.1:n.-15+50306G>A | |
ENST00000555855.5:c.-118+50306G>A | ENSP00000451135.1:n.-118+50306G>A | |
NM_001085471.1:c.-15+50306G>A | NP_001078940.1:n.-15+50306G>A | |
NM_001085471.2:c.-15+50306G>A | NP_001078940.1:n.-15+50306G>A |