Canonical Allele Identifier: CA1619378908

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951130G= , CM000668.2:g.31951130G=	GRCh38
NC_000006.11:g.31918907G= , CM000668.1:g.31918907G=	GRCh37
NC_000006.10:g.32026886G=	NCBI36
NG_008191.1:g.10187G= , LRG_136:g.10187G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-67G=
ENST00000483004.2:c.1640-14G=	ENSP00000419887.2:n.1640-14G=
ENST00000698628.1:c.1625-14G=	ENSP00000513848.1:n.1625-14G=
ENST00000698629.1:n.2128-67G=
ENST00000698630.1:n.2572-14G=
ENST00000698631.1:n.2573-14G=
ENST00000698632.1:n.3647G=
ENST00000698633.1:n.3537G=
ENST00000425368.7:c.1856-14G= MANE Select	ENSP00000416561.2:n.1856-14G=
ENST00000425368.6:c.1856-14G=	ENSP00000416561.2:n.1856-14G=
ENST00000456570.5:c.3362-14G=	ENSP00000410815.1:n.3362-14G=
ENST00000467360.1:n.982-14G=
ENST00000477310.1:c.2909-14G=	ENSP00000418996.1:n.2909-14G=
ENST00000482312.1:n.257G=
ENST00000483004.1:c.478-14G=
NM_001710.5:c.1856-14G= , LRG_136t1:c.1856-14G=	NP_001701.2:n.1856-14G=
NM_001710.6:c.1856-14G= MANE Select	NP_001701.2:n.1856-14G=