Canonical Allele Identifier: CA2578572574

Gene: CFB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946220C>T , CM000668.2:g.31946220C>T	GRCh38
NC_000006.11:g.31913997C>T , CM000668.1:g.31913997C>T	GRCh37
NC_000006.10:g.32021976C>T	NCBI36
NG_008191.1:g.5277C>T , LRG_136:g.5277C>T
NG_011730.1:g.23732C>T , LRG_26:g.23732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.176C>T
ENST00000483004.2:c.-2C>T	ENSP00000419887.2:n.-2C>T
ENST00000497841.6:c.-2C>T	ENSP00000513847.1:n.-2C>T
ENST00000698628.1:c.-2C>T	ENSP00000513848.1:n.-2C>T
ENST00000698629.1:n.176C>T
ENST00000698630.1:n.160C>T
ENST00000698631.1:n.155C>T
ENST00000698632.1:n.127C>T
ENST00000698633.1:n.97C>T
ENST00000698636.1:n.221C>T
ENST00000425368.7:c.-2C>T MANE Select	ENSP00000416561.2:n.-2C>T
ENST00000425368.6:c.-2C>T	ENSP00000416561.2:n.-2C>T
ENST00000456570.5:c.1571-153C>T	ENSP00000410815.1:n.1571-153C>T
ENST00000460718.5:c.-2C>T	ENSP00000417793.1:n.-2C>T
ENST00000472581.1:n.246C>T
ENST00000475617.5:c.-2C>T	ENSP00000420090.1:n.-2C>T
ENST00000477310.1:c.1352-787C>T	ENSP00000418996.1:n.1352-787C>T
NM_001710.5:c.-2C>T , LRG_136t1:c.-2C>T	NP_001701.2:n.-2C>T
NM_001710.6:c.-2C>T MANE Select	NP_001701.2:n.-2C>T