Canonical Allele Identifier: CA219086613
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs190980430
MyVariant Identifiers: chr11:g.22646494T>A (hg19) chr11:g.22624948T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624948T>A , CM000673.2:g.22624948T>A GRCh38
NC_000011.9:g.22646494T>A , CM000673.1:g.22646494T>A GRCh37
NC_000011.8:g.22603070T>A NCBI36
NG_007425.1:g.5894A>T , LRG_527:g.5894A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.863A>T MANE Select ENSP00000330875.3:p.Asp288Val
ENST00000327470.4:c.863A>T ENSP00000330875.3:p.Asp288Val
NM_022725.3:c.863A>T , LRG_527t1:c.863A>T NP_073562.1:p.Asp288Val
NM_022725.4:c.863A>T MANE Select NP_073562.1:p.Asp288Val
Search 100 bp 5'
Search 100 bp 3'