HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22062114G>T , CM000671.2:g.22062114G>T | GRCh38 |
NC_000009.11:g.22062113G>T , CM000671.1:g.22062113G>T | GRCh37 |
NC_000009.10:g.22052113G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2158+88G>T | ||
NR_047532.1:n.1075+5727G>T | ||
NR_047533.1:n.644+12886G>T | ||
NR_047534.1:n.644+12886G>T | ||
NR_047535.1:n.780+5727G>T | ||
NR_047536.1:n.644+12886G>T | ||
NR_047537.1:n.780+5727G>T | ||
NR_047538.1:n.644+12886G>T | ||
NR_047539.1:n.2158+88G>T | ||
NR_047540.1:n.854+88G>T | ||
NR_047541.1:n.781-1830G>T | ||
NR_047542.1:n.780+5727G>T | ||
NR_047543.1:n.780+5727G>T | ||
NR_120536.1:n.644+12886G>T |