HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22088083T>C , CM000671.2:g.22088083T>C | GRCh38 |
NC_000009.11:g.22088082T>C , CM000671.1:g.22088082T>C | GRCh37 |
NC_000009.10:g.22078082T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2449-8289T>C | ||
NR_047532.1:n.1076-4225T>C | ||
NR_047534.1:n.645-9175T>C | ||
NR_047535.1:n.781-24237T>C | ||
NR_047536.1:n.645-24237T>C | ||
NR_047537.1:n.780+31696T>C | ||
NR_047538.1:n.645-32117T>C | ||
NR_047543.1:n.781-24237T>C | ||
NR_120536.1:n.645-32421T>C |