Canonical Allele Identifier: CA2723416217
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1409758967
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625115del , CM000673.2:g.22625115del GRCh38
NC_000011.9:g.22646661del , CM000673.1:g.22646661del GRCh37
NC_000011.8:g.22603237del NCBI36
NG_007425.1:g.5730del , LRG_527:g.5730del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.699del MANE Select ENSP00000330875.3:p.Ser234AlafsTer4
ENST00000327470.4:c.699del ENSP00000330875.3:p.Ser234AlafsTer4
NM_022725.3:c.699del , LRG_527t1:c.699del NP_073562.1:p.Ser234AlafsTer4
NM_022725.4:c.699del MANE Select NP_073562.1:p.Ser234AlafsTer4
Search 100 bp 5'
Search 100 bp 3'