HGVS | Genome Assembly |
---|---|
NC_000011.10:g.113903386T>C , CM000673.2:g.113903386T>C | GRCh38 |
NC_000011.9:g.113774108T>C , CM000673.1:g.113774108T>C | GRCh37 |
NC_000011.8:g.113279318T>C | NCBI36 |
NG_011483.1:g.3520T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_011543064.1:c.12+4303T>C | XP_011541366.1:n.12+4303T>C | |
XM_024448767.1:c.-243+4303T>C | XP_024304535.1:n.-243+4303T>C |