Canonical Allele Identifier: CA219086637

Gene: FANCF

Linked Data

• dbSNP Id: rs865886264
• MyVariant Identifiers: chr11:g.22646783G>A (hg19) ; chr11:g.22625237G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22625237G>A , CM000673.2:g.22625237G>A	GRCh38
NC_000011.9:g.22646783G>A , CM000673.1:g.22646783G>A	GRCh37
NC_000011.8:g.22603359G>A	NCBI36
NG_007425.1:g.5605C>T , LRG_527:g.5605C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.574C>T MANE Select	ENSP00000330875.3:p.Leu192=
ENST00000327470.4:c.574C>T	ENSP00000330875.3:p.Leu192=
NM_022725.3:c.574C>T , LRG_527t1:c.574C>T	NP_073562.1:p.Leu192=
NM_022725.4:c.574C>T MANE Select	NP_073562.1:p.Leu192=