Canonical Allele Identifier: CA1619378885

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951100G= , CM000668.2:g.31951100G=	GRCh38
NC_000006.11:g.31918877G= , CM000668.1:g.31918877G=	GRCh37
NC_000006.10:g.32026856G=	NCBI36
NG_008191.1:g.10157G= , LRG_136:g.10157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-97G=
ENST00000483004.2:c.1640-44G=	ENSP00000419887.2:n.1640-44G=
ENST00000698628.1:c.1625-44G=	ENSP00000513848.1:n.1625-44G=
ENST00000698629.1:n.2128-97G=
ENST00000698630.1:n.2572-44G=
ENST00000698631.1:n.2573-44G=
ENST00000698632.1:n.3617G=
ENST00000698633.1:n.3507G=
ENST00000425368.7:c.1856-44G= MANE Select	ENSP00000416561.2:n.1856-44G=
ENST00000425368.6:c.1856-44G=	ENSP00000416561.2:n.1856-44G=
ENST00000456570.5:c.3362-44G=	ENSP00000410815.1:n.3362-44G=
ENST00000467360.1:n.982-44G=
ENST00000477310.1:c.2909-44G=	ENSP00000418996.1:n.2909-44G=
ENST00000482312.1:n.227G=
ENST00000483004.1:c.478-44G=
NM_001710.5:c.1856-44G= , LRG_136t1:c.1856-44G=	NP_001701.2:n.1856-44G=
NM_001710.6:c.1856-44G= MANE Select	NP_001701.2:n.1856-44G=