HGVS | Genome Assembly |
---|---|
NC_000022.11:g.21658553A>G , CM000684.2:g.21658553A>G | GRCh38 |
NC_000022.10:g.22012842A>G , CM000684.1:g.22012842A>G | GRCh37 |
NC_000022.9:g.20342842A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000641967.1:n.286+164A>G | ||
ENST00000498589.1:n.540-90A>G | ||
XM_017029165.1:c.674+91A>G | XP_016884654.1:n.674+91A>G | |
NR_169729.1:n.1365A>G | ||
NR_169730.1:n.1268A>G | ||
NR_169731.1:n.432-2284A>G | ||
NR_169732.1:n.328+91A>G | ||
NR_169733.1:n.387-90A>G | ||
NR_169734.1:n.411-90A>G |