HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34796553T>C , CM000677.2:g.34796553T>C | GRCh38 |
NC_000015.9:g.35088754T>C , CM000677.1:g.35088754T>C | GRCh37 |
NC_000015.8:g.32876046T>C | NCBI36 |
NG_007553.1:g.4174A>G , LRG_388:g.4174A>G |
HGVS | Amino-acid Change | |
---|---|---|
NR_120329.1:n.300-13943T>C |