Canonical Allele Identifier: CA1619374602

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946218C= , CM000668.2:g.31946218C=	GRCh38
NC_000006.11:g.31913995C= , CM000668.1:g.31913995C=	GRCh37
NC_000006.10:g.32021974C=	NCBI36
NG_008191.1:g.5275C= , LRG_136:g.5275C=
NG_011730.1:g.23730C= , LRG_26:g.23730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.174C=
ENST00000483004.2:c.-4C=	ENSP00000419887.2:n.-4C=
ENST00000497841.6:c.-4C=	ENSP00000513847.1:n.-4C=
ENST00000698628.1:c.-4C=	ENSP00000513848.1:n.-4C=
ENST00000698629.1:n.174C=
ENST00000698630.1:n.158C=
ENST00000698631.1:n.153C=
ENST00000698632.1:n.125C=
ENST00000698633.1:n.95C=
ENST00000698636.1:n.219C=
ENST00000425368.7:c.-4C= MANE Select	ENSP00000416561.2:n.-4C=
ENST00000425368.6:c.-4C=	ENSP00000416561.2:n.-4C=
ENST00000456570.5:c.1571-155C=	ENSP00000410815.1:n.1571-155C=
ENST00000460718.5:c.-4C=	ENSP00000417793.1:n.-4C=
ENST00000472581.1:n.244C=
ENST00000475617.5:c.-4C=	ENSP00000420090.1:n.-4C=
ENST00000477310.1:c.1352-789C=	ENSP00000418996.1:n.1352-789C=
NM_001710.5:c.-4C= , LRG_136t1:c.-4C=	NP_001701.2:n.-4C=
NM_001710.6:c.-4C= MANE Select	NP_001701.2:n.-4C=