HGVS | Genome Assembly |
---|---|
NC_000007.14:g.148807184T>C , CM000669.2:g.148807184T>C | GRCh38 |
NC_000007.13:g.148504276T>C , CM000669.1:g.148504276T>C | GRCh37 |
NC_000007.12:g.148135209T>C | NCBI36 |
NG_032043.1:g.82166A>G , LRG_531:g.82166A>G |
HGVS | Amino-acid Change | |
---|---|---|
XR_928101.1:n.515+2099T>C | ||
XR_928102.1:n.722+2099T>C |