Genomic Alleles
| 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 |
Transcript Alleles
| 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 |