Canonical Allele Identifier: CA219086608
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs959443639
gnomAD v2: 11-22646449-G-A
gnomAD v4: 11-22624903-G-A
MyVariant Identifiers: chr11:g.22646449G>A (hg19) chr11:g.22624903G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624903G>A , CM000673.2:g.22624903G>A GRCh38
NC_000011.9:g.22646449G>A , CM000673.1:g.22646449G>A GRCh37
NC_000011.8:g.22603025G>A NCBI36
NG_007425.1:g.5939C>T , LRG_527:g.5939C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.908C>T MANE Select ENSP00000330875.3:p.Pro303Leu
ENST00000327470.4:c.908C>T ENSP00000330875.3:p.Pro303Leu
NM_022725.3:c.908C>T , LRG_527t1:c.908C>T NP_073562.1:p.Pro303Leu
NM_022725.4:c.908C>T MANE Select NP_073562.1:p.Pro303Leu
Search 100 bp 5'
Search 100 bp 3'