Canonical Allele Identifier: CA380058123
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22624921-G-T
MyVariant Identifiers: chr11:g.22646467G>T (hg19) chr11:g.22624921G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624921G>T , CM000673.2:g.22624921G>T GRCh38
NC_000011.9:g.22646467G>T , CM000673.1:g.22646467G>T GRCh37
NC_000011.8:g.22603043G>T NCBI36
NG_007425.1:g.5921C>A , LRG_527:g.5921C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.890C>A MANE Select ENSP00000330875.3:p.Thr297Asn
ENST00000327470.4:c.890C>A ENSP00000330875.3:p.Thr297Asn
NM_022725.3:c.890C>A , LRG_527t1:c.890C>A NP_073562.1:p.Thr297Asn
NM_022725.4:c.890C>A MANE Select NP_073562.1:p.Thr297Asn
Search 100 bp 5'
Search 100 bp 3'