HGVS | Genome Assembly |
---|---|
NC_000016.10:g.75133681G>T , CM000678.2:g.75133681G>T | GRCh38 |
NC_000016.9:g.75167579G>T , CM000678.1:g.75167579G>T | GRCh37 |
NC_000016.8:g.73725080G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011522921.1:c.35+1059G>T | XP_011521223.1:n.35+1059G>T | |
XM_011522921.2:c.35+1059G>T | XP_011521223.1:n.35+1059G>T |