Canonical Allele Identifier: CA1619374687

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946361C= , CM000668.2:g.31946361C=	GRCh38
NC_000006.11:g.31914138C= , CM000668.1:g.31914138C=	GRCh37
NC_000006.10:g.32022117C=	NCBI36
NG_008191.1:g.5418C= , LRG_136:g.5418C=
NG_011730.1:g.23873C= , LRG_26:g.23873C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.242-12C=
ENST00000483004.2:c.65-12C=	ENSP00000419887.2:n.65-12C=
ENST00000497841.6:c.65-12C=	ENSP00000513847.1:n.65-12C=
ENST00000698628.1:c.65-12C=	ENSP00000513848.1:n.65-12C=
ENST00000698629.1:n.242-12C=
ENST00000698630.1:n.226-12C=
ENST00000698631.1:n.221-12C=
ENST00000698632.1:n.193-12C=
ENST00000698633.1:n.163-12C=
ENST00000698636.1:n.287-12C=
ENST00000425368.7:c.65-12C= MANE Select	ENSP00000416561.2:n.65-12C=
ENST00000425368.6:c.65-12C=	ENSP00000416561.2:n.65-12C=
ENST00000452035.6:n.65-12C=
ENST00000456570.5:c.1571-12C=	ENSP00000410815.1:n.1571-12C=
ENST00000460718.5:c.64+76C=	ENSP00000417793.1:n.64+76C=
ENST00000472581.1:n.312-12C=
ENST00000475617.5:c.65-12C=	ENSP00000420090.1:n.65-12C=
ENST00000477310.1:c.1352-646C=	ENSP00000418996.1:n.1352-646C=
NM_001710.5:c.65-12C= , LRG_136t1:c.65-12C=	NP_001701.2:n.65-12C=
NM_001710.6:c.65-12C= MANE Select	NP_001701.2:n.65-12C=