Canonical Allele Identifier: CA380059158
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22646975T>G (hg19) chr11:g.22625429T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625429T>G , CM000673.2:g.22625429T>G GRCh38
NC_000011.9:g.22646975T>G , CM000673.1:g.22646975T>G GRCh37
NC_000011.8:g.22603551T>G NCBI36
NG_007425.1:g.5413A>C , LRG_527:g.5413A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.382A>C MANE Select ENSP00000330875.3:p.Thr128Pro
ENST00000327470.4:c.382A>C ENSP00000330875.3:p.Thr128Pro
NM_022725.3:c.382A>C , LRG_527t1:c.382A>C NP_073562.1:p.Thr128Pro
NM_022725.4:c.382A>C MANE Select NP_073562.1:p.Thr128Pro
Search 100 bp 5'
Search 100 bp 3'