Canonical Allele Identifier: CA1619378875

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951083A= , CM000668.2:g.31951083A=	GRCh38
NC_000006.11:g.31918860A= , CM000668.1:g.31918860A=	GRCh37
NC_000006.10:g.32026839A=	NCBI36
NG_008191.1:g.10140A= , LRG_136:g.10140A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-114A=
ENST00000483004.2:c.1640-61A=	ENSP00000419887.2:n.1640-61A=
ENST00000698628.1:c.1625-61A=	ENSP00000513848.1:n.1625-61A=
ENST00000698629.1:n.2128-114A=
ENST00000698630.1:n.2572-61A=
ENST00000698631.1:n.2573-61A=
ENST00000698632.1:n.3600A=
ENST00000698633.1:n.3490A=
ENST00000425368.7:c.1856-61A= MANE Select	ENSP00000416561.2:n.1856-61A=
ENST00000425368.6:c.1856-61A=	ENSP00000416561.2:n.1856-61A=
ENST00000456570.5:c.3362-61A=	ENSP00000410815.1:n.3362-61A=
ENST00000467360.1:n.982-61A=
ENST00000477310.1:c.2909-61A=	ENSP00000418996.1:n.2909-61A=
ENST00000482312.1:n.210A=
ENST00000483004.1:c.478-61A=
NM_001710.5:c.1856-61A= , LRG_136t1:c.1856-61A=	NP_001701.2:n.1856-61A=
NM_001710.6:c.1856-61A= MANE Select	NP_001701.2:n.1856-61A=