HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22056551T>A , CM000671.2:g.22056551T>A | GRCh38 |
NC_000009.11:g.22056550T>A , CM000671.1:g.22056550T>A | GRCh37 |
NC_000009.10:g.22046550T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.1388+164T>A | ||
NR_047532.1:n.1075+164T>A | ||
NR_047533.1:n.644+7323T>A | ||
NR_047534.1:n.644+7323T>A | ||
NR_047535.1:n.780+164T>A | ||
NR_047536.1:n.644+7323T>A | ||
NR_047537.1:n.780+164T>A | ||
NR_047538.1:n.644+7323T>A | ||
NR_047539.1:n.1388+164T>A | ||
NR_047540.1:n.780+164T>A | ||
NR_047541.1:n.780+164T>A | ||
NR_047542.1:n.780+164T>A | ||
NR_047543.1:n.780+164T>A | ||
NR_120536.1:n.644+7323T>A |