HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133526985T>A , CM000672.2:g.133526985T>A | GRCh38 |
NC_000010.10:g.135340489T>A , CM000672.1:g.135340489T>A | GRCh37 |
NC_000010.9:g.135190479T>A | NCBI36 |
NG_008383.1:g.4623T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463117.6:c.-40+112T>A | ENSP00000440689.1:n.-40+112T>A | |
ENST00000541261.1:c.-40+112T>A | ENSP00000437799.1:n.-40+112T>A |