HGVS | Genome Assembly |
---|---|
NC_000009.12:g.22088136T>C , CM000671.2:g.22088136T>C | GRCh38 |
NC_000009.11:g.22088135T>C , CM000671.1:g.22088135T>C | GRCh37 |
NC_000009.10:g.22078135T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_003529.3:n.2449-8236T>C | ||
NR_047532.1:n.1076-4172T>C | ||
NR_047534.1:n.645-9122T>C | ||
NR_047535.1:n.781-24184T>C | ||
NR_047536.1:n.645-24184T>C | ||
NR_047537.1:n.780+31749T>C | ||
NR_047538.1:n.645-32064T>C | ||
NR_047543.1:n.781-24184T>C | ||
NR_120536.1:n.645-32368T>C |