Canonical Allele Identifier: CA380059017
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22646901T>G (hg19) chr11:g.22625355T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625355T>G , CM000673.2:g.22625355T>G GRCh38
NC_000011.9:g.22646901T>G , CM000673.1:g.22646901T>G GRCh37
NC_000011.8:g.22603477T>G NCBI36
NG_007425.1:g.5487A>C , LRG_527:g.5487A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.456A>C MANE Select ENSP00000330875.3:p.Arg152Ser
ENST00000327470.4:c.456A>C ENSP00000330875.3:p.Arg152Ser
NM_022725.3:c.456A>C , LRG_527t1:c.456A>C NP_073562.1:p.Arg152Ser
NM_022725.4:c.456A>C MANE Select NP_073562.1:p.Arg152Ser
Search 100 bp 5'
Search 100 bp 3'