HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6470995A>C , CM000674.2:g.6470995A>C | GRCh38 |
NC_000012.11:g.6580161A>C , CM000674.1:g.6580161A>C | GRCh37 |
NC_000012.10:g.6450422A>C | NCBI36 |
NG_042188.1:g.4905T>G | |
NG_042188.2:g.4905T>G |
HGVS | Amino-acid Change | |
---|---|---|
XR_001748777.2:n.2262A>C | ||
XR_001748778.2:n.2259A>C |