Canonical Allele Identifier: CA380058351
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22646582G>A (hg19) chr11:g.22625036G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625036G>A , CM000673.2:g.22625036G>A GRCh38
NC_000011.9:g.22646582G>A , CM000673.1:g.22646582G>A GRCh37
NC_000011.8:g.22603158G>A NCBI36
NG_007425.1:g.5806C>T , LRG_527:g.5806C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.775C>T MANE Select ENSP00000330875.3:p.Leu259Phe
ENST00000327470.4:c.775C>T ENSP00000330875.3:p.Leu259Phe
NM_022725.3:c.775C>T , LRG_527t1:c.775C>T NP_073562.1:p.Leu259Phe
NM_022725.4:c.775C>T MANE Select NP_073562.1:p.Leu259Phe
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