Canonical Allele Identifier: CA380059330
Gene: FANCF HGNC NCBI
GAS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22647064A>G (hg19) chr11:g.22625518A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625518A>G , CM000673.2:g.22625518A>G GRCh38
NC_000011.9:g.22647064A>G , CM000673.1:g.22647064A>G GRCh37
NC_000011.8:g.22603640A>G NCBI36
NG_007425.1:g.5324T>C , LRG_527:g.5324T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.293T>C (FANCF) MANE Select ENSP00000330875.3:p.Leu98Pro
ENST00000648096.1:n.10A>G (GAS2)
ENST00000327470.4:c.293T>C (FANCF) ENSP00000330875.3:p.Leu98Pro
NM_022725.3:c.293T>C , LRG_527t1:c.293T>C (FANCF) NP_073562.1:p.Leu98Pro
NM_022725.4:c.293T>C (FANCF) MANE Select NP_073562.1:p.Leu98Pro
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