Canonical Allele Identifier: CA913567761
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1565055110
gnomAD v2: 11-22646714-ACAAAGGCGGCTG-A
gnomAD v3: 11-22625168-ACAAAGGCGGCTG-A
gnomAD v4: 11-22625168-ACAAAGGCGGCTG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625172_22625183del , CM000673.2:g.22625172_22625183del GRCh38
NC_000011.9:g.22646718_22646729del , CM000673.1:g.22646718_22646729del GRCh37
NC_000011.8:g.22603294_22603305del NCBI36
NG_007425.1:g.5662_5673del , LRG_527:g.5662_5673del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.631_642del MANE Select ENSP00000330875.3:p.Gln211_Leu214del
ENST00000327470.4:c.631_642del ENSP00000330875.3:p.Gln211_Leu214del
NM_022725.3:c.631_642del , LRG_527t1:c.631_642del NP_073562.1:p.Gln211_Leu214del
NM_022725.4:c.631_642del MANE Select NP_073562.1:p.Gln211_Leu214del
Search 100 bp 5'
Search 100 bp 3'