Canonical Allele Identifier: CA380059718
Gene: FANCF HGNC NCBI
GAS2 HGNC NCBI

Linked Data

dbSNP Id: rs1180204445
gnomAD v4: 11-22625719-A-T
MyVariant Identifiers: chr11:g.22647265A>T (hg19) chr11:g.22625719A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625719A>T , CM000673.2:g.22625719A>T GRCh38
NC_000011.9:g.22647265A>T , CM000673.1:g.22647265A>T GRCh37
NC_000011.8:g.22603841A>T NCBI36
NG_007425.1:g.5123T>A , LRG_527:g.5123T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.92T>A (FANCF) MANE Select ENSP00000330875.3:p.Val31Glu
ENST00000648096.1:n.211A>T (GAS2)
ENST00000327470.4:c.92T>A (FANCF) ENSP00000330875.3:p.Val31Glu
ENST00000528582.5:c.-115A>T (GAS2) ENSP00000432584.1:n.-115A>T
NM_022725.3:c.92T>A , LRG_527t1:c.92T>A (FANCF) NP_073562.1:p.Val31Glu
NM_022725.4:c.92T>A (FANCF) MANE Select NP_073562.1:p.Val31Glu
Search 100 bp 5'
Search 100 bp 3'