HGVS | Genome Assembly |
---|---|
NC_000018.10:g.26866653T>C , CM000680.2:g.26866653T>C | GRCh38 |
NC_000018.9:g.24446617T>C , CM000680.1:g.24446617T>C | GRCh37 |
NC_000018.8:g.22700615T>C | NCBI36 |
NG_029560.1:g.4100A>G |
HGVS | Amino-acid Change | |
---|---|---|
NR_026908.1:n.53+1293T>C |