Canonical Allele Identifier: CA1957607193
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625427T= , CM000673.2:g.22625427T= GRCh38
NC_000011.9:g.22646973T= , CM000673.1:g.22646973T= GRCh37
NC_000011.8:g.22603549T= NCBI36
NG_007425.1:g.5415A= , LRG_527:g.5415A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.384A= MANE Select ENSP00000330875.3:p.Thr128=
ENST00000327470.4:c.384A= ENSP00000330875.3:p.Thr128=
NM_022725.3:c.384A= , LRG_527t1:c.384A= NP_073562.1:p.Thr128=
NM_022725.4:c.384A= MANE Select NP_073562.1:p.Thr128=