Canonical Allele Identifier: CA1619379290

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951520A= , CM000668.2:g.31951520A=	GRCh38
NC_000006.11:g.31919297A= , CM000668.1:g.31919297A=	GRCh37
NC_000006.10:g.32027276A=	NCBI36
NG_008191.1:g.10577A= , LRG_136:g.10577A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2524-35A=
ENST00000483004.2:c.1874-35A=	ENSP00000419887.2:n.1874-35A=
ENST00000698628.1:c.1859-35A=	ENSP00000513848.1:n.1859-35A=
ENST00000698629.1:n.2309-35A=
ENST00000698630.1:n.2806-35A=
ENST00000698631.1:n.2807-35A=
ENST00000698632.1:n.3895-35A=
ENST00000698633.1:n.3785-35A=
ENST00000425368.7:c.2090-35A= MANE Select	ENSP00000416561.2:n.2090-35A=
ENST00000425368.6:c.2090-35A=	ENSP00000416561.2:n.2090-35A=
ENST00000456570.5:c.3596-35A=	ENSP00000410815.1:n.3596-35A=
ENST00000477310.1:c.3143-35A=	ENSP00000418996.1:n.3143-35A=
ENST00000482312.1:n.505-35A=
ENST00000483004.1:c.712-35A=
ENST00000498317.1:c.60-35A=
NM_001710.5:c.2090-35A= , LRG_136t1:c.2090-35A=	NP_001701.2:n.2090-35A=
NM_001710.6:c.2090-35A= MANE Select	NP_001701.2:n.2090-35A=