Canonical Allele Identifier: CA1957607195
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625429T= , CM000673.2:g.22625429T= GRCh38
NC_000011.9:g.22646975T= , CM000673.1:g.22646975T= GRCh37
NC_000011.8:g.22603551T= NCBI36
NG_007425.1:g.5413A= , LRG_527:g.5413A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.382A= MANE Select ENSP00000330875.3:p.Thr128=
ENST00000327470.4:c.382A= ENSP00000330875.3:p.Thr128=
NM_022725.3:c.382A= , LRG_527t1:c.382A= NP_073562.1:p.Thr128=
NM_022725.4:c.382A= MANE Select NP_073562.1:p.Thr128=
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