HGVS | Genome Assembly |
---|---|
NC_000002.12:g.111246290T>C , CM000664.2:g.111246290T>C | GRCh38 |
NC_000002.11:g.112003867T>C , CM000664.1:g.112003867T>C | GRCh37 |
NC_000002.10:g.111720338T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011512259.1:c.-309+1858A>G | XP_011510561.1:n.-309+1858A>G | |
XM_011512260.1:c.-114+1858A>G | XP_011510562.1:n.-114+1858A>G | |
XM_011512261.1:c.-2+1858A>G | XP_011510563.1:n.-2+1858A>G | |
NR_015395.2:n.2470-6294A>G | ||
NR_136161.1:n.637+1858A>G | ||
NR_136162.1:n.2470-12551A>G | ||
NR_136163.1:n.637+1858A>G | ||
NR_136164.1:n.544-37629A>G | ||
NR_136165.1:n.548+1858A>G | ||
NR_136166.1:n.2470-12551A>G |