Canonical Allele Identifier: CA5924377
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs775367657
ExAC: 11:22647049 A / T
gnomAD v2: 11-22647049-A-T
gnomAD v4: 11-22625503-A-T
MyVariant Identifiers: chr11:g.22647049A>T (hg19) chr11:g.22625503A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625503A>T , CM000673.2:g.22625503A>T GRCh38
NC_000011.9:g.22647049A>T , CM000673.1:g.22647049A>T GRCh37
NC_000011.8:g.22603625A>T NCBI36
NG_007425.1:g.5339T>A , LRG_527:g.5339T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.308T>A MANE Select ENSP00000330875.3:p.Leu103His
ENST00000327470.4:c.308T>A ENSP00000330875.3:p.Leu103His
NM_022725.3:c.308T>A , LRG_527t1:c.308T>A NP_073562.1:p.Leu103His
NM_022725.4:c.308T>A MANE Select NP_073562.1:p.Leu103His
Search 100 bp 5'
Search 100 bp 3'