Canonical Allele Identifier: CA473533506
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625298-C-A
MyVariant Identifiers: chr11:g.22646844C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625298C>A , CM000673.2:g.22625298C>A GRCh38
NC_000011.9:g.22646844C>A , CM000673.1:g.22646844C>A GRCh37
NC_000011.8:g.22603420C>A NCBI36
NG_007425.1:g.5544G>T , LRG_527:g.5544G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.513G>T MANE Select ENSP00000330875.3:p.Leu171=
ENST00000327470.4:c.513G>T ENSP00000330875.3:p.Leu171=
NM_022725.3:c.513G>T , LRG_527t1:c.513G>T NP_073562.1:p.Leu171=
NM_022725.4:c.513G>T MANE Select NP_073562.1:p.Leu171=
Search 100 bp 5'
Search 100 bp 3'