HGVS | Genome Assembly |
---|---|
NC_000015.10:g.93271900T>C , CM000677.2:g.93271900T>C | GRCh38 |
NC_000015.9:g.93815129T>C , CM000677.1:g.93815129T>C | GRCh37 |
NC_000015.8:g.91616133T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_932628.1:n.229+12663T>C | ||
XR_001751669.1:n.229+12663T>C |