Canonical Allele Identifier: CA473533669
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797964
MyVariant Identifiers: chr11:g.22646994G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625448G>C , CM000673.2:g.22625448G>C GRCh38
NC_000011.9:g.22646994G>C , CM000673.1:g.22646994G>C GRCh37
NC_000011.8:g.22603570G>C NCBI36
NG_007425.1:g.5394C>G , LRG_527:g.5394C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.363C>G MANE Select ENSP00000330875.3:p.Val121=
ENST00000327470.4:c.363C>G ENSP00000330875.3:p.Val121=
NM_022725.3:c.363C>G , LRG_527t1:c.363C>G NP_073562.1:p.Val121=
NM_022725.4:c.363C>G MANE Select NP_073562.1:p.Val121=
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