Canonical Allele Identifier: CA935897590
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v3: 11-22623980-G-A
gnomAD v4: 11-22623980-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22623980G>A , CM000673.2:g.22623980G>A GRCh38
NC_000011.9:g.22645526G>A , CM000673.1:g.22645526G>A GRCh37
NC_000011.8:g.22602102G>A NCBI36
NG_007425.1:g.6862C>T , LRG_527:g.6862C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.*706C>T MANE Select ENSP00000330875.3:n.*706C>T
ENST00000327470.4:c.*706C>T ENSP00000330875.3:n.*706C>T
NM_022725.3:c.*706C>T , LRG_527t1:c.*706C>T NP_073562.1:n.*706C>T
NM_022725.4:c.*706C>T MANE Select NP_073562.1:n.*706C>T
Search 100 bp 5'
Search 100 bp 3'