Canonical Allele Identifier: CA380058627
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs769318926
MyVariant Identifiers: chr11:g.22646716A>T (hg19) chr11:g.22625170A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625170A>T , CM000673.2:g.22625170A>T GRCh38
NC_000011.9:g.22646716A>T , CM000673.1:g.22646716A>T GRCh37
NC_000011.8:g.22603292A>T NCBI36
NG_007425.1:g.5672T>A , LRG_527:g.5672T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.641T>A MANE Select ENSP00000330875.3:p.Leu214Ter
ENST00000327470.4:c.641T>A ENSP00000330875.3:p.Leu214Ter
NM_022725.3:c.641T>A , LRG_527t1:c.641T>A NP_073562.1:p.Leu214Ter
NM_022725.4:c.641T>A MANE Select NP_073562.1:p.Leu214Ter
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