Canonical Allele Identifier: CA1619374600

Gene: CFB

Linked Data

• dbSNP Id: rs561556943

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946217A>T , CM000668.2:g.31946217A>T	GRCh38
NC_000006.11:g.31913994A>T , CM000668.1:g.31913994A>T	GRCh37
NC_000006.10:g.32021973A>T	NCBI36
NG_008191.1:g.5274A>T , LRG_136:g.5274A>T
NG_011730.1:g.23729A>T , LRG_26:g.23729A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.173A>T
ENST00000483004.2:c.-5A>T	ENSP00000419887.2:n.-5A>T
ENST00000497841.6:c.-5A>T	ENSP00000513847.1:n.-5A>T
ENST00000698628.1:c.-5A>T	ENSP00000513848.1:n.-5A>T
ENST00000698629.1:n.173A>T
ENST00000698630.1:n.157A>T
ENST00000698631.1:n.152A>T
ENST00000698632.1:n.124A>T
ENST00000698633.1:n.94A>T
ENST00000698636.1:n.218A>T
ENST00000425368.7:c.-5A>T MANE Select	ENSP00000416561.2:n.-5A>T
ENST00000425368.6:c.-5A>T	ENSP00000416561.2:n.-5A>T
ENST00000456570.5:c.1571-156A>T	ENSP00000410815.1:n.1571-156A>T
ENST00000460718.5:c.-5A>T	ENSP00000417793.1:n.-5A>T
ENST00000472581.1:n.243A>T
ENST00000475617.5:c.-5A>T	ENSP00000420090.1:n.-5A>T
ENST00000477310.1:c.1352-790A>T	ENSP00000418996.1:n.1352-790A>T
NM_001710.5:c.-5A>T , LRG_136t1:c.-5A>T	NP_001701.2:n.-5A>T
NM_001710.6:c.-5A>T MANE Select	NP_001701.2:n.-5A>T