HGVS | Genome Assembly |
---|---|
NC_000018.10:g.26866578T>C , CM000680.2:g.26866578T>C | GRCh38 |
NC_000018.9:g.24446542T>C , CM000680.1:g.24446542T>C | GRCh37 |
NC_000018.8:g.22700540T>C | NCBI36 |
NG_029560.1:g.4175A>G |
HGVS | Amino-acid Change | |
---|---|---|
NR_026908.1:n.53+1218T>C |