HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22115028T>G , CM000671.2:g.22115028T>G | GRCh38 |
NC_000009.11:g.22115027T>G , CM000671.1:g.22115027T>G | GRCh37 |
NC_000009.10:g.22105027T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2908+1229T>G | ||
NR_047532.1:n.1697+1229T>G | ||
NR_047534.1:n.961+1229T>G | ||
NR_047535.1:n.856+2633T>G | ||
NR_047536.1:n.720+2633T>G | ||
NR_047537.1:n.781-5172T>G | ||
NR_047538.1:n.645-5172T>G | ||
NR_047543.1:n.990+1229T>G | ||
NR_120536.1:n.645-5476T>G |