Linked Data
MyVariant Identifiers:
chr11:g.22647264C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625718C>A , CM000673.2:g.22625718C>A | GRCh38 |
| NC_000011.9:g.22647264C>A , CM000673.1:g.22647264C>A | GRCh37 |
| NC_000011.8:g.22603840C>A | NCBI36 |
| NG_007425.1:g.5124G>T , LRG_527:g.5124G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.93G>T (FANCF) MANE Select | ENSP00000330875.3:p.Val31= | |
| ENST00000648096.1:n.210C>A (GAS2) | ||
| ENST00000327470.4:c.93G>T (FANCF) | ENSP00000330875.3:p.Val31= | |
| ENST00000528582.5:c.-116C>A (GAS2) | ENSP00000432584.1:n.-116C>A | |
| NM_022725.3:c.93G>T , LRG_527t1:c.93G>T (FANCF) | NP_073562.1:p.Val31= | |
| NM_022725.4:c.93G>T (FANCF) MANE Select | NP_073562.1:p.Val31= |