HGVS | Genome Assembly |
---|---|
NC_000005.10:g.60491911G>C , CM000667.2:g.60491911G>C | GRCh38 |
NC_000005.9:g.59787738G>C , CM000667.1:g.59787738G>C | GRCh37 |
NC_000005.8:g.59823495G>C | NCBI36 |
NG_027957.1:g.1188C>G | |
NG_027957.2:g.37419C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506510.6:n.70+30140C>G (PDE4D) | ||
NR_024617.1:n.711+3488G>C (PART1) | ||
NR_028509.1:n.492+3488G>C (PART1) | ||
XM_011543472.1:c.-90+30140C>G (PDE4D) | XP_011541774.1:n.-90+30140C>G | |
NM_001364599.1:c.-90+4228C>G (PDE4D) | NP_001351528.1:n.-90+4228C>G | |
XM_024446110.1:c.-90+30140C>G (PDE4D) | XP_024301878.1:n.-90+30140C>G | |
XM_024446112.1:c.-90+30140C>G (PDE4D) | XP_024301880.1:n.-90+30140C>G |