Canonical Allele Identifier: CA380058469
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22646639A>T (hg19) chr11:g.22625093A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625093A>T , CM000673.2:g.22625093A>T GRCh38
NC_000011.9:g.22646639A>T , CM000673.1:g.22646639A>T GRCh37
NC_000011.8:g.22603215A>T NCBI36
NG_007425.1:g.5749T>A , LRG_527:g.5749T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.718T>A MANE Select ENSP00000330875.3:p.Trp240Arg
ENST00000327470.4:c.718T>A ENSP00000330875.3:p.Trp240Arg
NM_022725.3:c.718T>A , LRG_527t1:c.718T>A NP_073562.1:p.Trp240Arg
NM_022725.4:c.718T>A MANE Select NP_073562.1:p.Trp240Arg
Search 100 bp 5'
Search 100 bp 3'