Canonical Allele Identifier: CA380058882
Gene: FANCF HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.517C>T MANE Select ENSP00000330875.3:p.Arg173Cys
ENST00000327470.4:c.517C>T ENSP00000330875.3:p.Arg173Cys
NM_022725.3:c.517C>T , LRG_527t1:c.517C>T NP_073562.1:p.Arg173Cys
NM_022725.4:c.517C>T MANE Select NP_073562.1:p.Arg173Cys
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Search 100 bp 3'