Canonical Allele Identifier: CA1619378358

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950474C= , CM000668.2:g.31950474C=	GRCh38
NC_000006.11:g.31918251C= , CM000668.1:g.31918251C=	GRCh37
NC_000006.10:g.32026230C=	NCBI36
NG_008191.1:g.9531C= , LRG_136:g.9531C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.1872C=
ENST00000483004.2:c.1409-145C=	ENSP00000419887.2:n.1409-145C=
ENST00000698628.1:c.1624+71C=	ENSP00000513848.1:n.1624+71C=
ENST00000698629.1:n.1801+71C=
ENST00000698630.1:n.2340+71C=
ENST00000698631.1:n.2341+71C=
ENST00000698632.1:n.2991C=
ENST00000698633.1:n.2881C=
ENST00000698636.1:n.1846+71C=
ENST00000425368.7:c.1624+71C= MANE Select	ENSP00000416561.2:n.1624+71C=
ENST00000425368.6:c.1624+71C=	ENSP00000416561.2:n.1624+71C=
ENST00000452035.6:n.1695C=
ENST00000456570.5:c.3130+71C=	ENSP00000410815.1:n.3130+71C=
ENST00000467360.1:n.606C=
ENST00000477310.1:c.2677+71C=	ENSP00000418996.1:n.2677+71C=
ENST00000483004.1:c.247-145C=
NM_001710.5:c.1624+71C= , LRG_136t1:c.1624+71C=	NP_001701.2:n.1624+71C=
NM_001710.6:c.1624+71C= MANE Select	NP_001701.2:n.1624+71C=