Canonical Allele Identifier: CA380059116
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797855
gnomAD v3: 11-22625408-G-A
gnomAD v4: 11-22625408-G-A
MyVariant Identifiers: chr11:g.22646954G>A (hg19) chr11:g.22625408G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625408G>A , CM000673.2:g.22625408G>A GRCh38
NC_000011.9:g.22646954G>A , CM000673.1:g.22646954G>A GRCh37
NC_000011.8:g.22603530G>A NCBI36
NG_007425.1:g.5434C>T , LRG_527:g.5434C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.403C>T MANE Select ENSP00000330875.3:p.Arg135Cys
ENST00000327470.4:c.403C>T ENSP00000330875.3:p.Arg135Cys
NM_022725.3:c.403C>T , LRG_527t1:c.403C>T NP_073562.1:p.Arg135Cys
NM_022725.4:c.403C>T MANE Select NP_073562.1:p.Arg135Cys
Search 100 bp 5'
Search 100 bp 3'