HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22114508G>T , CM000671.2:g.22114508G>T | GRCh38 |
NC_000009.11:g.22114507G>T , CM000671.1:g.22114507G>T | GRCh37 |
NC_000009.10:g.22104507G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2908+709G>T | ||
NR_047532.1:n.1697+709G>T | ||
NR_047534.1:n.961+709G>T | ||
NR_047535.1:n.856+2113G>T | ||
NR_047536.1:n.720+2113G>T | ||
NR_047537.1:n.781-5692G>T | ||
NR_047538.1:n.645-5692G>T | ||
NR_047543.1:n.990+709G>T | ||
NR_120536.1:n.645-5996G>T |