HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22061955A>T , CM000671.2:g.22061955A>T | GRCh38 |
NC_000009.11:g.22061954A>T , CM000671.1:g.22061954A>T | GRCh37 |
NC_000009.10:g.22051954A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2087A>T | ||
NR_047532.1:n.1075+5568A>T | ||
NR_047533.1:n.644+12727A>T | ||
NR_047534.1:n.644+12727A>T | ||
NR_047535.1:n.780+5568A>T | ||
NR_047536.1:n.644+12727A>T | ||
NR_047537.1:n.780+5568A>T | ||
NR_047538.1:n.644+12727A>T | ||
NR_047539.1:n.2087A>T | ||
NR_047540.1:n.783A>T | ||
NR_047541.1:n.781-1989A>T | ||
NR_047542.1:n.780+5568A>T | ||
NR_047543.1:n.780+5568A>T | ||
NR_120536.1:n.644+12727A>T |