HGVS | Genome Assembly |
---|---|
NC_000006.12:g.159061489C>T , CM000668.2:g.159061489C>T | GRCh38 |
NC_000006.11:g.159482521C>T , CM000668.1:g.159482521C>T | GRCh37 |
NC_000006.10:g.159402509C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011536288.1:c.621+2092G>A | XP_011534590.1:n.621+2092G>A | |
XM_011536289.1:c.507+2092G>A | XP_011534591.1:n.507+2092G>A | |
XM_024446608.1:c.*1626G>A | XP_024302376.1:n.*1626G>A | |
XR_001744430.2:n.1247-5750C>T |