Canonical Allele Identifier: CA2678071864

Gene: CFB

Linked Data

• gnomAD v4: 6-31946205-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946205T>A , CM000668.2:g.31946205T>A	GRCh38
NC_000006.11:g.31913982T>A , CM000668.1:g.31913982T>A	GRCh37
NC_000006.10:g.32021961T>A	NCBI36
NG_008191.1:g.5262T>A , LRG_136:g.5262T>A
NG_011730.1:g.23717T>A , LRG_26:g.23717T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.161T>A
ENST00000483004.2:c.-17T>A	ENSP00000419887.2:n.-17T>A
ENST00000497841.6:c.-17T>A	ENSP00000513847.1:n.-17T>A
ENST00000698628.1:c.-17T>A	ENSP00000513848.1:n.-17T>A
ENST00000698629.1:n.161T>A
ENST00000698630.1:n.145T>A
ENST00000698631.1:n.140T>A
ENST00000698632.1:n.112T>A
ENST00000698633.1:n.82T>A
ENST00000698636.1:n.206T>A
ENST00000425368.7:c.-17T>A MANE Select	ENSP00000416561.2:n.-17T>A
ENST00000425368.6:c.-17T>A	ENSP00000416561.2:n.-17T>A
ENST00000456570.5:c.1571-168T>A	ENSP00000410815.1:n.1571-168T>A
ENST00000460718.5:c.-17T>A	ENSP00000417793.1:n.-17T>A
ENST00000472581.1:n.231T>A
ENST00000475617.5:c.-17T>A	ENSP00000420090.1:n.-17T>A
ENST00000477310.1:c.1352-802T>A	ENSP00000418996.1:n.1352-802T>A
NM_001710.5:c.-17T>A , LRG_136t1:c.-17T>A	NP_001701.2:n.-17T>A
NM_001710.6:c.-17T>A MANE Select	NP_001701.2:n.-17T>A