HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22116176T>A , CM000671.2:g.22116176T>A | GRCh38 |
NC_000009.11:g.22116175T>A , CM000671.1:g.22116175T>A | GRCh37 |
NC_000009.10:g.22106175T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.2908+2377T>A | ||
NR_047532.1:n.1697+2377T>A | ||
NR_047534.1:n.961+2377T>A | ||
NR_047535.1:n.857-2468T>A | ||
NR_047536.1:n.721-2468T>A | ||
NR_047537.1:n.781-4024T>A | ||
NR_047538.1:n.645-4024T>A | ||
NR_047543.1:n.990+2377T>A | ||
NR_120536.1:n.645-4328T>A |