Canonical Allele Identifier: CA380058569
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797140
MyVariant Identifiers: chr11:g.22646688T>A (hg19) chr11:g.22625142T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625142T>A , CM000673.2:g.22625142T>A GRCh38
NC_000011.9:g.22646688T>A , CM000673.1:g.22646688T>A GRCh37
NC_000011.8:g.22603264T>A NCBI36
NG_007425.1:g.5700A>T , LRG_527:g.5700A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.669A>T MANE Select ENSP00000330875.3:p.Glu223Asp
ENST00000327470.4:c.669A>T ENSP00000330875.3:p.Glu223Asp
NM_022725.3:c.669A>T , LRG_527t1:c.669A>T NP_073562.1:p.Glu223Asp
NM_022725.4:c.669A>T MANE Select NP_073562.1:p.Glu223Asp
Search 100 bp 5'
Search 100 bp 3'