Canonical Allele Identifier: CA1619378876

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951087G= , CM000668.2:g.31951087G=	GRCh38
NC_000006.11:g.31918864G= , CM000668.1:g.31918864G=	GRCh37
NC_000006.10:g.32026843G=	NCBI36
NG_008191.1:g.10144G= , LRG_136:g.10144G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-110G=
ENST00000483004.2:c.1640-57G=	ENSP00000419887.2:n.1640-57G=
ENST00000698628.1:c.1625-57G=	ENSP00000513848.1:n.1625-57G=
ENST00000698629.1:n.2128-110G=
ENST00000698630.1:n.2572-57G=
ENST00000698631.1:n.2573-57G=
ENST00000698632.1:n.3604G=
ENST00000698633.1:n.3494G=
ENST00000425368.7:c.1856-57G= MANE Select	ENSP00000416561.2:n.1856-57G=
ENST00000425368.6:c.1856-57G=	ENSP00000416561.2:n.1856-57G=
ENST00000456570.5:c.3362-57G=	ENSP00000410815.1:n.3362-57G=
ENST00000467360.1:n.982-57G=
ENST00000477310.1:c.2909-57G=	ENSP00000418996.1:n.2909-57G=
ENST00000482312.1:n.214G=
ENST00000483004.1:c.478-57G=
NM_001710.5:c.1856-57G= , LRG_136t1:c.1856-57G=	NP_001701.2:n.1856-57G=
NM_001710.6:c.1856-57G= MANE Select	NP_001701.2:n.1856-57G=