Canonical Allele Identifier: CA380058881
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs764066836
MyVariant Identifiers: chr11:g.22646839C>T (hg19) chr11:g.22625293C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625293C>T , CM000673.2:g.22625293C>T GRCh38
NC_000011.9:g.22646839C>T , CM000673.1:g.22646839C>T GRCh37
NC_000011.8:g.22603415C>T NCBI36
NG_007425.1:g.5549G>A , LRG_527:g.5549G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.518G>A MANE Select ENSP00000330875.3:p.Arg173His
ENST00000327470.4:c.518G>A ENSP00000330875.3:p.Arg173His
NM_022725.3:c.518G>A , LRG_527t1:c.518G>A NP_073562.1:p.Arg173His
NM_022725.4:c.518G>A MANE Select NP_073562.1:p.Arg173His
Search 100 bp 5'
Search 100 bp 3'