HGVS | Genome Assembly |
---|---|
NC_000014.9:g.78068563G>C , CM000676.2:g.78068563G>C | GRCh38 |
NC_000014.8:g.78534906G>C , CM000676.1:g.78534906G>C | GRCh37 |
NC_000014.7:g.77604659G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011537364.1:c.-704+6242G>C | XP_011535666.1:n.-704+6242G>C | |
XM_011537364.2:c.-704+6242G>C | XP_011535666.1:n.-704+6242G>C | |
XM_017021790.1:c.-704+6242G>C | XP_016877279.1:n.-704+6242G>C | |
XM_017021791.1:c.-704+6242G>C | XP_016877280.1:n.-704+6242G>C |