Canonical Allele Identifier: CA219086620
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs34028937
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625039dup , CM000673.2:g.22625039dup GRCh38
NC_000011.9:g.22646585dup , CM000673.1:g.22646585dup GRCh37
NC_000011.8:g.22603161dup NCBI36
NG_007425.1:g.5805dup , LRG_527:g.5805dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.774dup MANE Select ENSP00000330875.3:p.Leu259AlafsTer7
ENST00000327470.4:c.774dup ENSP00000330875.3:p.Leu259AlafsTer7
NM_022725.3:c.774dup , LRG_527t1:c.774dup NP_073562.1:p.Leu259AlafsTer7
NM_022725.4:c.774dup MANE Select NP_073562.1:p.Leu259AlafsTer7
Search 100 bp 5'
Search 100 bp 3'