HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32634229T>G , CM000668.2:g.32634229T>G | GRCh38 |
NC_000006.11:g.32602006T>G , CM000668.1:g.32602006T>G | GRCh37 |
NC_000006.10:g.32709984T>G | NCBI36 |
NG_032876.1:g.1824T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000422863.1:c.-39+1320T>G | ENSP00000405797.1:n.-39+1320T>G |