Canonical Allele Identifier: CA380059186
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1590541791
MyVariant Identifiers: chr11:g.22646986G>T (hg19) chr11:g.22625440G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625440G>T , CM000673.2:g.22625440G>T GRCh38
NC_000011.9:g.22646986G>T , CM000673.1:g.22646986G>T GRCh37
NC_000011.8:g.22603562G>T NCBI36
NG_007425.1:g.5402C>A , LRG_527:g.5402C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.371C>A MANE Select ENSP00000330875.3:p.Ala124Asp
ENST00000327470.4:c.371C>A ENSP00000330875.3:p.Ala124Asp
NM_022725.3:c.371C>A , LRG_527t1:c.371C>A NP_073562.1:p.Ala124Asp
NM_022725.4:c.371C>A MANE Select NP_073562.1:p.Ala124Asp
Search 100 bp 5'
Search 100 bp 3'