Canonical Allele Identifier: CA1619378869

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951078G= , CM000668.2:g.31951078G=	GRCh38
NC_000006.11:g.31918855G= , CM000668.1:g.31918855G=	GRCh37
NC_000006.10:g.32026834G=	NCBI36
NG_008191.1:g.10135G= , LRG_136:g.10135G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-119G=
ENST00000483004.2:c.1640-66G=	ENSP00000419887.2:n.1640-66G=
ENST00000698628.1:c.1625-66G=	ENSP00000513848.1:n.1625-66G=
ENST00000698629.1:n.2128-119G=
ENST00000698630.1:n.2572-66G=
ENST00000698631.1:n.2573-66G=
ENST00000698632.1:n.3595G=
ENST00000698633.1:n.3485G=
ENST00000425368.7:c.1856-66G= MANE Select	ENSP00000416561.2:n.1856-66G=
ENST00000425368.6:c.1856-66G=	ENSP00000416561.2:n.1856-66G=
ENST00000456570.5:c.3362-66G=	ENSP00000410815.1:n.3362-66G=
ENST00000467360.1:n.982-66G=
ENST00000477310.1:c.2909-66G=	ENSP00000418996.1:n.2909-66G=
ENST00000482312.1:n.205G=
ENST00000483004.1:c.478-66G=
NM_001710.5:c.1856-66G= , LRG_136t1:c.1856-66G=	NP_001701.2:n.1856-66G=
NM_001710.6:c.1856-66G= MANE Select	NP_001701.2:n.1856-66G=