Canonical Allele Identifier: CA380059182
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs61752920
MyVariant Identifiers: chr11:g.22646984C>A (hg19) chr11:g.22625438C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625438C>A , CM000673.2:g.22625438C>A GRCh38
NC_000011.9:g.22646984C>A , CM000673.1:g.22646984C>A GRCh37
NC_000011.8:g.22603560C>A NCBI36
NG_007425.1:g.5404G>T , LRG_527:g.5404G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.373G>T MANE Select ENSP00000330875.3:p.Asp125Tyr
ENST00000327470.4:c.373G>T ENSP00000330875.3:p.Asp125Tyr
NM_022725.3:c.373G>T , LRG_527t1:c.373G>T NP_073562.1:p.Asp125Tyr
NM_022725.4:c.373G>T MANE Select NP_073562.1:p.Asp125Tyr
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Search 100 bp 3'