Linked Data
gnomAD v4:
11-22625521-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625521A>G , CM000673.2:g.22625521A>G | GRCh38 |
| NC_000011.9:g.22647067A>G , CM000673.1:g.22647067A>G | GRCh37 |
| NC_000011.8:g.22603643A>G | NCBI36 |
| NG_007425.1:g.5321T>C , LRG_527:g.5321T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.290T>C (FANCF) MANE Select | ENSP00000330875.3:p.Leu97Pro | |
| ENST00000648096.1:n.13A>G (GAS2) | ||
| ENST00000327470.4:c.290T>C (FANCF) | ENSP00000330875.3:p.Leu97Pro | |
| NM_022725.3:c.290T>C , LRG_527t1:c.290T>C (FANCF) | NP_073562.1:p.Leu97Pro | |
| NM_022725.4:c.290T>C (FANCF) MANE Select | NP_073562.1:p.Leu97Pro |