Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625570C>A , CM000673.2:g.22625570C>A | GRCh38 |
| NC_000011.9:g.22647116C>A , CM000673.1:g.22647116C>A | GRCh37 |
| NC_000011.8:g.22603692C>A | NCBI36 |
| NG_007425.1:g.5272G>T , LRG_527:g.5272G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022725.4:c.241G>T (FANCF) MANE Select | NP_073562.1:p.Ala81Ser |
| ENST00000327470.6:c.241G>T (FANCF) MANE Select | ENSP00000330875.3:p.Ala81Ser |
| NM_022725.3:c.241G>T , LRG_527t1:c.241G>T (FANCF) | NP_073562.1:p.Ala81Ser |
| ENST00000327470.4:c.241G>T (FANCF) | ENSP00000330875.3:p.Ala81Ser |
| ENST00000648096.1:n.62C>A (GAS2) |