Canonical Allele Identifier: CA1619374609

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946223T= , CM000668.2:g.31946223T=	GRCh38
NC_000006.11:g.31914000T= , CM000668.1:g.31914000T=	GRCh37
NC_000006.10:g.32021979T=	NCBI36
NG_008191.1:g.5280T= , LRG_136:g.5280T=
NG_011730.1:g.23735T= , LRG_26:g.23735T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.179T=
ENST00000483004.2:c.2T=	ENSP00000419887.2:p.Met1=
ENST00000497841.6:c.2T=	ENSP00000513847.1:p.Met1=
ENST00000698628.1:c.2T=	ENSP00000513848.1:p.Met1=
ENST00000698629.1:n.179T=
ENST00000698630.1:n.163T=
ENST00000698631.1:n.158T=
ENST00000698632.1:n.130T=
ENST00000698633.1:n.100T=
ENST00000698636.1:n.224T=
ENST00000425368.7:c.2T= MANE Select	ENSP00000416561.2:p.Met1=
ENST00000425368.6:c.2T=	ENSP00000416561.2:p.Met1=
ENST00000452035.6:n.2T=
ENST00000456570.5:c.1571-150T=	ENSP00000410815.1:n.1571-150T=
ENST00000460718.5:c.2T=	ENSP00000417793.1:p.Met1=
ENST00000472581.1:n.249T=
ENST00000475617.5:c.2T=	ENSP00000420090.1:p.Met1=
ENST00000477310.1:c.1352-784T=	ENSP00000418996.1:n.1352-784T=
NM_001710.5:c.2T= , LRG_136t1:c.2T=	NP_001701.2:p.Met1=
NM_001710.6:c.2T= MANE Select	NP_001701.2:p.Met1=