Canonical Allele Identifier: CA1619374907

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946627G= , CM000668.2:g.31946627G=	GRCh38
NC_000006.11:g.31914404G= , CM000668.1:g.31914404G=	GRCh37
NC_000006.10:g.32022383G=	NCBI36
NG_008191.1:g.5684G= , LRG_136:g.5684G=
NG_011730.1:g.24139G= , LRG_26:g.24139G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.475+21G=
ENST00000483004.2:c.298+21G=	ENSP00000419887.2:n.298+21G=
ENST00000497841.6:c.298+21G=	ENSP00000513847.1:n.298+21G=
ENST00000698628.1:c.298+21G=	ENSP00000513848.1:n.298+21G=
ENST00000698629.1:n.475+21G=
ENST00000698630.1:n.480G=
ENST00000698631.1:n.475G=
ENST00000698632.1:n.447G=
ENST00000698633.1:n.417G=
ENST00000698636.1:n.520+21G=
ENST00000425368.7:c.298+21G= MANE Select	ENSP00000416561.2:n.298+21G=
ENST00000425368.6:c.298+21G=	ENSP00000416561.2:n.298+21G=
ENST00000452035.6:n.298+21G=
ENST00000456570.5:c.1804+21G=	ENSP00000410815.1:n.1804+21G=
ENST00000460718.5:c.185+21G=	ENSP00000417793.1:n.185+21G=
ENST00000472581.1:n.566G=
ENST00000475617.5:c.298+21G=	ENSP00000420090.1:n.298+21G=
ENST00000477310.1:c.1352-380G=	ENSP00000418996.1:n.1352-380G=
NM_001710.5:c.298+21G= , LRG_136t1:c.298+21G=	NP_001701.2:n.298+21G=
NM_001710.6:c.298+21G= MANE Select	NP_001701.2:n.298+21G=