Canonical Allele Identifier: CA340605

Gene: FANCG

Linked Data

• ClinVar Variation Id: 6716
• ClinVar RCV Id: RCV000007108
• dbSNP Id: rs397507561
• MyVariant Identifiers: chr9:g.35076582T>C (hg19) ; chr9:g.35076585T>C (hg38)
• PubMed: PMID:12552564 ; PMID:20301575

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076585T>C , CM000671.2:g.35076585T>C	GRCh38
NC_000009.11:g.35076582T>C , CM000671.1:g.35076582T>C	GRCh37
NC_000009.10:g.35066582T>C	NCBI36
NG_007312.1:g.8432A>G , LRG_499:g.8432A>G
NG_007887.1:g.1158A>G , LRG_657:g.1158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.925-2A>G	ENSP00000409607.2:n.925-2A>G
ENST00000461149.2:n.2142-2A>G
ENST00000696700.1:n.2177-2A>G
ENST00000696701.1:n.1029-2A>G
ENST00000696702.1:c.*401-2A>G	ENSP00000512821.1:n.*401-2A>G
ENST00000696703.1:c.*401-2A>G	ENSP00000512822.1:n.*401-2A>G
ENST00000696706.1:n.988-2A>G
ENST00000696707.1:n.1142-2A>G
ENST00000696708.1:c.*270-2A>G	ENSP00000512825.1:n.*270-2A>G
ENST00000696709.1:n.1327-2A>G
ENST00000696710.1:c.925-2A>G	ENSP00000512826.1:n.925-2A>G
ENST00000696711.1:n.2374-2A>G
ENST00000696712.1:n.1041-2A>G
ENST00000696713.1:c.925-2A>G	ENSP00000512827.1:n.925-2A>G
ENST00000696714.1:n.1401-2A>G
ENST00000696715.1:c.925-2A>G	ENSP00000512828.1:n.925-2A>G
ENST00000378643.8:c.925-2A>G MANE Select	ENSP00000367910.4:n.925-2A>G
ENST00000378643.7:c.925-2A>G	ENSP00000367910.3:n.925-2A>G
ENST00000425676.5:c.*401-2A>G	ENSP00000412793.1:n.*401-2A>G
ENST00000474894.1:n.130-2A>G
NM_004629.1:c.925-2A>G , LRG_499t1:c.925-2A>G	NP_004620.1:n.925-2A>G
NM_004629.2:c.925-2A>G MANE Select	NP_004620.1:n.925-2A>G