Canonical Allele Identifier: CA2612850371
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22623886-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22623886T>G , CM000673.2:g.22623886T>G GRCh38
NC_000011.9:g.22645432T>G , CM000673.1:g.22645432T>G GRCh37
NC_000011.8:g.22602008T>G NCBI36
NG_007425.1:g.6956A>C , LRG_527:g.6956A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.*800A>C MANE Select ENSP00000330875.3:n.*800A>C
ENST00000327470.4:c.*800A>C ENSP00000330875.3:n.*800A>C
NM_022725.3:c.*800A>C , LRG_527t1:c.*800A>C NP_073562.1:n.*800A>C
NM_022725.4:c.*800A>C MANE Select NP_073562.1:n.*800A>C
Search 100 bp 5'
Search 100 bp 3'