HGVS | Genome Assembly |
---|---|
NC_000006.12:g.465985T>C , CM000668.2:g.465985T>C | GRCh38 |
NC_000006.11:g.465985T>C , CM000668.1:g.465985T>C | GRCh37 |
NC_000006.10:g.410985T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XR_926364.1:n.2714+12260T>C | ||
XR_926365.1:n.2548+12260T>C | ||
XR_001743914.1:n.482-9223T>C |