Canonical Allele Identifier: CA473533768
Gene: FANCF HGNC NCBI
GAS2 HGNC NCBI

Linked Data

dbSNP Id: rs761672325
gnomAD v3: 11-22625523-G-T
gnomAD v4: 11-22625523-G-T
MyVariant Identifiers: chr11:g.22647069G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625523G>T , CM000673.2:g.22625523G>T GRCh38
NC_000011.9:g.22647069G>T , CM000673.1:g.22647069G>T GRCh37
NC_000011.8:g.22603645G>T NCBI36
NG_007425.1:g.5319C>A , LRG_527:g.5319C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.288C>A (FANCF) MANE Select ENSP00000330875.3:p.Arg96=
ENST00000648096.1:n.15G>T (GAS2)
ENST00000327470.4:c.288C>A (FANCF) ENSP00000330875.3:p.Arg96=
NM_022725.3:c.288C>A , LRG_527t1:c.288C>A (FANCF) NP_073562.1:p.Arg96=
NM_022725.4:c.288C>A (FANCF) MANE Select NP_073562.1:p.Arg96=
Search 100 bp 5'
Search 100 bp 3'