HGVS | Genome Assembly |
---|---|
NC_000013.11:g.27855601T>C , CM000675.2:g.27855601T>C | GRCh38 |
NC_000013.10:g.28429738T>C , CM000675.1:g.28429738T>C | GRCh37 |
NC_000013.9:g.27327738T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_047484.1:n.242-7065A>G | ||
NR_047484.2:n.143-7065A>G |