Canonical Allele Identifier: CA473533709
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22647026G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625480G>A , CM000673.2:g.22625480G>A GRCh38
NC_000011.9:g.22647026G>A , CM000673.1:g.22647026G>A GRCh37
NC_000011.8:g.22603602G>A NCBI36
NG_007425.1:g.5362C>T , LRG_527:g.5362C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.331C>T MANE Select ENSP00000330875.3:p.Leu111=
ENST00000327470.4:c.331C>T ENSP00000330875.3:p.Leu111=
NM_022725.3:c.331C>T , LRG_527t1:c.331C>T NP_073562.1:p.Leu111=
NM_022725.4:c.331C>T MANE Select NP_073562.1:p.Leu111=
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