Canonical Allele Identifier: CA5924233

Gene: FANCF

Linked Data

• dbSNP Id: rs774102674
• ExAC: 11:22646447 A / T
• gnomAD v3: 11-22624901-A-T
• gnomAD v4: 11-22624901-A-T
• MyVariant Identifiers: chr11:g.22646447A>T (hg19) ; chr11:g.22624901A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22624901A>T , CM000673.2:g.22624901A>T	GRCh38
NC_000011.9:g.22646447A>T , CM000673.1:g.22646447A>T	GRCh37
NC_000011.8:g.22603023A>T	NCBI36
NG_007425.1:g.5941T>A , LRG_527:g.5941T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.910T>A MANE Select	ENSP00000330875.3:p.Trp304Arg
ENST00000327470.4:c.910T>A	ENSP00000330875.3:p.Trp304Arg
NM_022725.3:c.910T>A , LRG_527t1:c.910T>A	NP_073562.1:p.Trp304Arg
NM_022725.4:c.910T>A MANE Select	NP_073562.1:p.Trp304Arg