Canonical Allele Identifier: CA2678074420

Gene: CFB

Linked Data

• gnomAD v4: 6-31950987-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950987G>A , CM000668.2:g.31950987G>A	GRCh38
NC_000006.11:g.31918764G>A , CM000668.1:g.31918764G>A	GRCh37
NC_000006.10:g.32026743G>A	NCBI36
NG_008191.1:g.10044G>A , LRG_136:g.10044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2342+43G>A
ENST00000483004.2:c.1639+43G>A	ENSP00000419887.2:n.1639+43G>A
ENST00000698628.1:c.1625-157G>A	ENSP00000513848.1:n.1625-157G>A
ENST00000698629.1:n.2127+43G>A
ENST00000698630.1:n.2571+43G>A
ENST00000698631.1:n.2572+43G>A
ENST00000698632.1:n.3504G>A
ENST00000698633.1:n.3394G>A
ENST00000425368.7:c.1855+43G>A MANE Select	ENSP00000416561.2:n.1855+43G>A
ENST00000425368.6:c.1855+43G>A	ENSP00000416561.2:n.1855+43G>A
ENST00000456570.5:c.3361+43G>A	ENSP00000410815.1:n.3361+43G>A
ENST00000467360.1:n.981+43G>A
ENST00000477310.1:c.2908+43G>A	ENSP00000418996.1:n.2908+43G>A
ENST00000482312.1:n.114G>A
ENST00000483004.1:c.477+43G>A
NM_001710.5:c.1855+43G>A , LRG_136t1:c.1855+43G>A	NP_001701.2:n.1855+43G>A
NM_001710.6:c.1855+43G>A MANE Select	NP_001701.2:n.1855+43G>A