Canonical Allele Identifier: CA5924341
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs751463547
ExAC: 11:22646946 G / A
gnomAD v2: 11-22646946-G-A
gnomAD v4: 11-22625400-G-A
MyVariant Identifiers: chr11:g.22646946G>A (hg19) chr11:g.22625400G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625400G>A , CM000673.2:g.22625400G>A GRCh38
NC_000011.9:g.22646946G>A , CM000673.1:g.22646946G>A GRCh37
NC_000011.8:g.22603522G>A NCBI36
NG_007425.1:g.5442C>T , LRG_527:g.5442C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.411C>T MANE Select ENSP00000330875.3:p.Ala137=
ENST00000327470.4:c.411C>T ENSP00000330875.3:p.Ala137=
NM_022725.3:c.411C>T , LRG_527t1:c.411C>T NP_073562.1:p.Ala137=
NM_022725.4:c.411C>T MANE Select NP_073562.1:p.Ala137=
Search 100 bp 5'
Search 100 bp 3'