Canonical Allele Identifier: CA380058883
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797565
MyVariant Identifiers: chr11:g.22646840G>C (hg19) chr11:g.22625294G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625294G>C , CM000673.2:g.22625294G>C GRCh38
NC_000011.9:g.22646840G>C , CM000673.1:g.22646840G>C GRCh37
NC_000011.8:g.22603416G>C NCBI36
NG_007425.1:g.5548C>G , LRG_527:g.5548C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.517C>G MANE Select ENSP00000330875.3:p.Arg173Gly
ENST00000327470.4:c.517C>G ENSP00000330875.3:p.Arg173Gly
NM_022725.3:c.517C>G , LRG_527t1:c.517C>G NP_073562.1:p.Arg173Gly
NM_022725.4:c.517C>G MANE Select NP_073562.1:p.Arg173Gly
Search 100 bp 5'
Search 100 bp 3'