Canonical Allele Identifier: CA1619379502

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951818T= , CM000668.2:g.31951818T=	GRCh38
NC_000006.11:g.31919595T= , CM000668.1:g.31919595T=	GRCh37
NC_000006.10:g.32027574T=	NCBI36
NG_008191.1:g.10875T= , LRG_136:g.10875T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2574-57T=
ENST00000483004.2:c.1924-57T=	ENSP00000419887.2:n.1924-57T=
ENST00000698628.1:c.1909-57T=	ENSP00000513848.1:n.1909-57T=
ENST00000698629.1:n.2359-57T=
ENST00000698630.1:n.2856-57T=
ENST00000698631.1:n.2857-57T=
ENST00000698632.1:n.3945-57T=
ENST00000698633.1:n.3835-57T=
ENST00000425368.7:c.2140-57T= MANE Select	ENSP00000416561.2:n.2140-57T=
ENST00000425368.6:c.2140-57T=	ENSP00000416561.2:n.2140-57T=
ENST00000456570.5:c.3646-57T=	ENSP00000410815.1:n.3646-57T=
ENST00000477310.1:c.3193-57T=	ENSP00000418996.1:n.3193-57T=
ENST00000482312.1:n.555-57T=
ENST00000483004.1:c.762-57T=
ENST00000498317.1:c.323T=
NM_001710.5:c.2140-57T= , LRG_136t1:c.2140-57T=	NP_001701.2:n.2140-57T=
NM_001710.6:c.2140-57T= MANE Select	NP_001701.2:n.2140-57T=