Canonical Allele Identifier: CA1619378705

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950821T= , CM000668.2:g.31950821T=	GRCh38
NC_000006.11:g.31918598T= , CM000668.1:g.31918598T=	GRCh37
NC_000006.10:g.32026577T=	NCBI36
NG_008191.1:g.9878T= , LRG_136:g.9878T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2219T=
ENST00000483004.2:c.1563-47T=	ENSP00000419887.2:n.1563-47T=
ENST00000698628.1:c.1625-323T=	ENSP00000513848.1:n.1625-323T=
ENST00000698629.1:n.2004T=
ENST00000698630.1:n.2495-47T=
ENST00000698631.1:n.2496-47T=
ENST00000698632.1:n.3338T=
ENST00000698633.1:n.3228T=
ENST00000425368.7:c.1779-47T= MANE Select	ENSP00000416561.2:n.1779-47T=
ENST00000425368.6:c.1779-47T=	ENSP00000416561.2:n.1779-47T=
ENST00000456570.5:c.3285-47T=	ENSP00000410815.1:n.3285-47T=
ENST00000467360.1:n.905-47T=
ENST00000477310.1:c.2832-47T=	ENSP00000418996.1:n.2832-47T=
ENST00000483004.1:c.401-47T=
NM_001710.5:c.1779-47T= , LRG_136t1:c.1779-47T=	NP_001701.2:n.1779-47T=
NM_001710.6:c.1779-47T= MANE Select	NP_001701.2:n.1779-47T=