HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48303645A>C , CM000675.2:g.48303645A>C | GRCh38 |
NC_000013.10:g.48877781A>C , CM000675.1:g.48877781A>C | GRCh37 |
NC_000013.9:g.47775782A>C | NCBI36 |
NG_009009.1:g.4899A>C , LRG_517:g.4899A>C |
HGVS | Amino-acid Change | |
---|---|---|
NR_046414.1:n.17T>G | ||
NR_046414.2:n.58T>G |