Canonical Allele Identifier: CA2612850367
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22623885-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22623885T>A , CM000673.2:g.22623885T>A GRCh38
NC_000011.9:g.22645431T>A , CM000673.1:g.22645431T>A GRCh37
NC_000011.8:g.22602007T>A NCBI36
NG_007425.1:g.6957A>T , LRG_527:g.6957A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.*801A>T MANE Select ENSP00000330875.3:n.*801A>T
ENST00000327470.4:c.*801A>T ENSP00000330875.3:n.*801A>T
NM_022725.3:c.*801A>T , LRG_527t1:c.*801A>T NP_073562.1:n.*801A>T
NM_022725.4:c.*801A>T MANE Select NP_073562.1:n.*801A>T
Search 100 bp 5'
Search 100 bp 3'