HGVS | Genome Assembly |
---|---|
NC_000017.11:g.33643464C>G , CM000679.2:g.33643464C>G | GRCh38 |
NC_000017.10:g.31970483C>G , CM000679.1:g.31970483C>G | GRCh37 |
NC_000017.9:g.28994596C>G | NCBI36 |
NG_029763.1:g.518343G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000359872.6:c.555+512514G>C | ENSP00000352934.6:n.555+512514G>C | |
NM_001094.4:c.555+512514G>C | NP_001085.2:n.555+512514G>C | |
NM_001094.5:c.555+512514G>C | NP_001085.2:n.555+512514G>C |