HGVS | Genome Assembly |
---|---|
NC_000014.9:g.68807119T>C , CM000676.2:g.68807119T>C | GRCh38 |
NC_000014.8:g.69273836T>C , CM000676.1:g.69273836T>C | GRCh37 |
NC_000014.7:g.68343589T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011537441.1:c.673-465A>G | XP_011535743.1:n.673-465A>G | |
XM_011537442.1:c.673-465A>G | XP_011535744.1:n.673-465A>G | |
XM_011537443.1:c.673-465A>G | XP_011535745.1:n.673-465A>G |