Canonical Allele Identifier: CA473533500
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797546
MyVariant Identifiers: chr11:g.22646835C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625289C>A , CM000673.2:g.22625289C>A GRCh38
NC_000011.9:g.22646835C>A , CM000673.1:g.22646835C>A GRCh37
NC_000011.8:g.22603411C>A NCBI36
NG_007425.1:g.5553G>T , LRG_527:g.5553G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.522G>T MANE Select ENSP00000330875.3:p.Leu174=
ENST00000327470.4:c.522G>T ENSP00000330875.3:p.Leu174=
NM_022725.3:c.522G>T , LRG_527t1:c.522G>T NP_073562.1:p.Leu174=
NM_022725.4:c.522G>T MANE Select NP_073562.1:p.Leu174=
Search 100 bp 5'
Search 100 bp 3'