HGVS | Genome Assembly |
---|---|
NC_000011.10:g.94493959C>T , CM000673.2:g.94493959C>T | GRCh38 |
NC_000011.9:g.94227125C>T , CM000673.1:g.94227125C>T | GRCh37 |
NC_000011.8:g.93866773C>T | NCBI36 |
NG_007261.1:g.4916G>A , LRG_85:g.4916G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000544612.5:c.-167C>T (ANKRD49) | ENSP00000440396.1:n.-167C>T | |
XM_011542837.1:c.-105-1053G>A (MRE11) | XP_011541139.1:n.-105-1053G>A | |
XM_011542837.2:c.-105-1053G>A (MRE11) | XP_011541139.1:n.-105-1053G>A |