HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22114396T>C , CM000671.2:g.22114396T>C | GRCh38 |
NC_000009.11:g.22114395T>C , CM000671.1:g.22114395T>C | GRCh37 |
NC_000009.10:g.22104395T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2908+597T>C | ||
NR_047532.1:n.1697+597T>C | ||
NR_047534.1:n.961+597T>C | ||
NR_047535.1:n.856+2001T>C | ||
NR_047536.1:n.720+2001T>C | ||
NR_047537.1:n.781-5804T>C | ||
NR_047538.1:n.645-5804T>C | ||
NR_047543.1:n.990+597T>C | ||
NR_120536.1:n.645-6108T>C |