Canonical Allele Identifier: CA2678074455

Gene: CFB

Linked Data

• gnomAD v4: 6-31951077-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31951077A>G , CM000668.2:g.31951077A>G	GRCh38
NC_000006.11:g.31918854A>G , CM000668.1:g.31918854A>G	GRCh37
NC_000006.10:g.32026833A>G	NCBI36
NG_008191.1:g.10134A>G , LRG_136:g.10134A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2343-120A>G
ENST00000483004.2:c.1640-67A>G	ENSP00000419887.2:n.1640-67A>G
ENST00000698628.1:c.1625-67A>G	ENSP00000513848.1:n.1625-67A>G
ENST00000698629.1:n.2128-120A>G
ENST00000698630.1:n.2572-67A>G
ENST00000698631.1:n.2573-67A>G
ENST00000698632.1:n.3594A>G
ENST00000698633.1:n.3484A>G
ENST00000425368.7:c.1856-67A>G MANE Select	ENSP00000416561.2:n.1856-67A>G
ENST00000425368.6:c.1856-67A>G	ENSP00000416561.2:n.1856-67A>G
ENST00000456570.5:c.3362-67A>G	ENSP00000410815.1:n.3362-67A>G
ENST00000467360.1:n.982-67A>G
ENST00000477310.1:c.2909-67A>G	ENSP00000418996.1:n.2909-67A>G
ENST00000482312.1:n.204A>G
ENST00000483004.1:c.478-67A>G
NM_001710.5:c.1856-67A>G , LRG_136t1:c.1856-67A>G	NP_001701.2:n.1856-67A>G
NM_001710.6:c.1856-67A>G MANE Select	NP_001701.2:n.1856-67A>G