HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22114912T>C , CM000671.2:g.22114912T>C | GRCh38 |
NC_000009.11:g.22114911T>C , CM000671.1:g.22114911T>C | GRCh37 |
NC_000009.10:g.22104911T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_003529.3:n.2908+1113T>C | ||
NR_047532.1:n.1697+1113T>C | ||
NR_047534.1:n.961+1113T>C | ||
NR_047535.1:n.856+2517T>C | ||
NR_047536.1:n.720+2517T>C | ||
NR_047537.1:n.781-5288T>C | ||
NR_047538.1:n.645-5288T>C | ||
NR_047543.1:n.990+1113T>C | ||
NR_120536.1:n.645-5592T>C |