Canonical Allele Identifier: CA1087492833

Gene: CFB

Linked Data

• dbSNP Id: rs1771732787
• gnomAD v3: 6-31951101-A-G
• gnomAD v4: 6-31951101-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951101A>G , CM000668.2:g.31951101A>G	GRCh38
NC_000006.11:g.31918878A>G , CM000668.1:g.31918878A>G	GRCh37
NC_000006.10:g.32026857A>G	NCBI36
NG_008191.1:g.10158A>G , LRG_136:g.10158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-96A>G
ENST00000483004.2:c.1640-43A>G	ENSP00000419887.2:n.1640-43A>G
ENST00000698628.1:c.1625-43A>G	ENSP00000513848.1:n.1625-43A>G
ENST00000698629.1:n.2128-96A>G
ENST00000698630.1:n.2572-43A>G
ENST00000698631.1:n.2573-43A>G
ENST00000698632.1:n.3618A>G
ENST00000698633.1:n.3508A>G
ENST00000425368.7:c.1856-43A>G MANE Select	ENSP00000416561.2:n.1856-43A>G
ENST00000425368.6:c.1856-43A>G	ENSP00000416561.2:n.1856-43A>G
ENST00000456570.5:c.3362-43A>G	ENSP00000410815.1:n.3362-43A>G
ENST00000467360.1:n.982-43A>G
ENST00000477310.1:c.2909-43A>G	ENSP00000418996.1:n.2909-43A>G
ENST00000482312.1:n.228A>G
ENST00000483004.1:c.478-43A>G
NM_001710.5:c.1856-43A>G , LRG_136t1:c.1856-43A>G	NP_001701.2:n.1856-43A>G
NM_001710.6:c.1856-43A>G MANE Select	NP_001701.2:n.1856-43A>G