Canonical Allele Identifier: CA380059249
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625476-A-C
MyVariant Identifiers: chr11:g.22647022A>C (hg19) chr11:g.22625476A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625476A>C , CM000673.2:g.22625476A>C GRCh38
NC_000011.9:g.22647022A>C , CM000673.1:g.22647022A>C GRCh37
NC_000011.8:g.22603598A>C NCBI36
NG_007425.1:g.5366T>G , LRG_527:g.5366T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.335T>G MANE Select ENSP00000330875.3:p.Val112Gly
ENST00000327470.4:c.335T>G ENSP00000330875.3:p.Val112Gly
NM_022725.3:c.335T>G , LRG_527t1:c.335T>G NP_073562.1:p.Val112Gly
NM_022725.4:c.335T>G MANE Select NP_073562.1:p.Val112Gly
Search 100 bp 5'
Search 100 bp 3'