HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22088088T>C , CM000671.2:g.22088088T>C | GRCh38 |
NC_000009.11:g.22088087T>C , CM000671.1:g.22088087T>C | GRCh37 |
NC_000009.10:g.22078087T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2449-8284T>C | ||
NR_047532.1:n.1076-4220T>C | ||
NR_047534.1:n.645-9170T>C | ||
NR_047535.1:n.781-24232T>C | ||
NR_047536.1:n.645-24232T>C | ||
NR_047537.1:n.780+31701T>C | ||
NR_047538.1:n.645-32112T>C | ||
NR_047543.1:n.781-24232T>C | ||
NR_120536.1:n.645-32416T>C |