Canonical Allele Identifier: CA473533818
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625190-C-T
MyVariant Identifiers: chr11:g.22646736C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625190C>T , CM000673.2:g.22625190C>T GRCh38
NC_000011.9:g.22646736C>T , CM000673.1:g.22646736C>T GRCh37
NC_000011.8:g.22603312C>T NCBI36
NG_007425.1:g.5652G>A , LRG_527:g.5652G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.621G>A MANE Select ENSP00000330875.3:p.Val207=
ENST00000327470.4:c.621G>A ENSP00000330875.3:p.Val207=
NM_022725.3:c.621G>A , LRG_527t1:c.621G>A NP_073562.1:p.Val207=
NM_022725.4:c.621G>A MANE Select NP_073562.1:p.Val207=
Search 100 bp 5'
Search 100 bp 3'