HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32634398T>A , CM000668.2:g.32634398T>A | GRCh38 |
NC_000006.11:g.32602175T>A , CM000668.1:g.32602175T>A | GRCh37 |
NC_000006.10:g.32710153T>A | NCBI36 |
NG_032876.1:g.1993T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000422863.1:c.-39+1489T>A | ENSP00000405797.1:n.-39+1489T>A |