Canonical Allele Identifier: CA380058961
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625331-G-C
COSMIC: COSM6068331
MyVariant Identifiers: chr11:g.22646877G>C (hg19) chr11:g.22625331G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625331G>C , CM000673.2:g.22625331G>C GRCh38
NC_000011.9:g.22646877G>C , CM000673.1:g.22646877G>C GRCh37
NC_000011.8:g.22603453G>C NCBI36
NG_007425.1:g.5511C>G , LRG_527:g.5511C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.480C>G MANE Select ENSP00000330875.3:p.Asp160Glu
ENST00000327470.4:c.480C>G ENSP00000330875.3:p.Asp160Glu
NM_022725.3:c.480C>G , LRG_527t1:c.480C>G NP_073562.1:p.Asp160Glu
NM_022725.4:c.480C>G MANE Select NP_073562.1:p.Asp160Glu
Search 100 bp 5'
Search 100 bp 3'