Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625722G>A , CM000673.2:g.22625722G>A | GRCh38 |
| NC_000011.9:g.22647268G>A , CM000673.1:g.22647268G>A | GRCh37 |
| NC_000011.8:g.22603844G>A | NCBI36 |
| NG_007425.1:g.5120C>T , LRG_527:g.5120C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.89C>T (FANCF) MANE Select | ENSP00000330875.3:p.Thr30Ile | |
| ENST00000648096.1:n.214G>A (GAS2) | ||
| ENST00000327470.4:c.89C>T (FANCF) | ENSP00000330875.3:p.Thr30Ile | |
| ENST00000528582.5:c.-112G>A (GAS2) | ENSP00000432584.1:n.-112G>A | |
| NM_022725.3:c.89C>T , LRG_527t1:c.89C>T (FANCF) | NP_073562.1:p.Thr30Ile | |
| NM_022725.4:c.89C>T (FANCF) MANE Select | NP_073562.1:p.Thr30Ile |