HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22116072T>A , CM000671.2:g.22116072T>A | GRCh38 |
NC_000009.11:g.22116071T>A , CM000671.1:g.22116071T>A | GRCh37 |
NC_000009.10:g.22106071T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.2908+2273T>A | ||
NR_047532.1:n.1697+2273T>A | ||
NR_047534.1:n.961+2273T>A | ||
NR_047535.1:n.857-2572T>A | ||
NR_047536.1:n.721-2572T>A | ||
NR_047537.1:n.781-4128T>A | ||
NR_047538.1:n.645-4128T>A | ||
NR_047543.1:n.990+2273T>A | ||
NR_120536.1:n.645-4432T>A |