Canonical Allele Identifier: CA5924376
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs771023850

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625493T>G , CM000673.2:g.22625493T>G GRCh38
NC_000011.9:g.22647039T>G , CM000673.1:g.22647039T>G GRCh37
NC_000011.8:g.22603615T>G NCBI36
NG_007425.1:g.5349A>C , LRG_527:g.5349A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.318A>C MANE Select ENSP00000330875.3:p.Ala106=
ENST00000327470.4:c.318A>C ENSP00000330875.3:p.Ala106=
NM_022725.3:c.318A>C , LRG_527t1:c.318A>C NP_073562.1:p.Ala106=
NM_022725.4:c.318A>C MANE Select NP_073562.1:p.Ala106=