Canonical Allele Identifier: CA1619378722

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950835G= , CM000668.2:g.31950835G=	GRCh38
NC_000006.11:g.31918612G= , CM000668.1:g.31918612G=	GRCh37
NC_000006.10:g.32026591G=	NCBI36
NG_008191.1:g.9892G= , LRG_136:g.9892G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2233G=
ENST00000483004.2:c.1563-33G=	ENSP00000419887.2:n.1563-33G=
ENST00000698628.1:c.1625-309G=	ENSP00000513848.1:n.1625-309G=
ENST00000698629.1:n.2018G=
ENST00000698630.1:n.2495-33G=
ENST00000698631.1:n.2496-33G=
ENST00000698632.1:n.3352G=
ENST00000698633.1:n.3242G=
ENST00000425368.7:c.1779-33G= MANE Select	ENSP00000416561.2:n.1779-33G=
ENST00000425368.6:c.1779-33G=	ENSP00000416561.2:n.1779-33G=
ENST00000456570.5:c.3285-33G=	ENSP00000410815.1:n.3285-33G=
ENST00000467360.1:n.905-33G=
ENST00000477310.1:c.2832-33G=	ENSP00000418996.1:n.2832-33G=
ENST00000483004.1:c.401-33G=
NM_001710.5:c.1779-33G= , LRG_136t1:c.1779-33G=	NP_001701.2:n.1779-33G=
NM_001710.6:c.1779-33G= MANE Select	NP_001701.2:n.1779-33G=