Canonical Allele Identifier: CA674709463
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1457408838
gnomAD v3: 11-22625441-CGTCCCGGACGCCCGGGCCGGGAAAGAG-C
gnomAD v4: 11-22625441-CGTCCCGGACGCCCGGGCCGGGAAAGAG-C
MyVariant Identifiers: chr11:g.22646988_22647014del (hg19) chr11:g.22625442_22625468del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625442_22625468del , CM000673.2:g.22625442_22625468del GRCh38
NC_000011.9:g.22646988_22647014del , CM000673.1:g.22646988_22647014del GRCh37
NC_000011.8:g.22603564_22603590del NCBI36
NG_007425.1:g.5374_5400del , LRG_527:g.5374_5400del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.343_369del MANE Select ENSP00000330875.3:p.Leu115_Asp123del
ENST00000327470.4:c.343_369del ENSP00000330875.3:p.Leu115_Asp123del
NM_022725.3:c.343_369del , LRG_527t1:c.343_369del NP_073562.1:p.Leu115_Asp123del
NM_022725.4:c.343_369del MANE Select NP_073562.1:p.Leu115_Asp123del
Search 100 bp 5'
Search 100 bp 3'