HGVS | Genome Assembly |
---|---|
NC_000004.12:g.102499922C>G , CM000666.2:g.102499922C>G | GRCh38 |
NC_000004.11:g.103421079C>G , CM000666.1:g.103421079C>G | GRCh37 |
NC_000004.10:g.103640111C>G | NCBI36 |
NG_050628.1:g.3594C>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011532467.1:c.643+1327G>C | XP_011530769.1:n.643+1327G>C | |
NR_136202.1:n.48+2517G>C |