Canonical Allele Identifier: CA1619378828

Gene: CFB

Linked Data

• dbSNP Id: rs1771726982

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950999A>G , CM000668.2:g.31950999A>G	GRCh38
NC_000006.11:g.31918776A>G , CM000668.1:g.31918776A>G	GRCh37
NC_000006.10:g.32026755A>G	NCBI36
NG_008191.1:g.10056A>G , LRG_136:g.10056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2342+55A>G
ENST00000483004.2:c.1639+55A>G	ENSP00000419887.2:n.1639+55A>G
ENST00000698628.1:c.1625-145A>G	ENSP00000513848.1:n.1625-145A>G
ENST00000698629.1:n.2127+55A>G
ENST00000698630.1:n.2571+55A>G
ENST00000698631.1:n.2572+55A>G
ENST00000698632.1:n.3516A>G
ENST00000698633.1:n.3406A>G
ENST00000425368.7:c.1855+55A>G MANE Select	ENSP00000416561.2:n.1855+55A>G
ENST00000425368.6:c.1855+55A>G	ENSP00000416561.2:n.1855+55A>G
ENST00000456570.5:c.3361+55A>G	ENSP00000410815.1:n.3361+55A>G
ENST00000467360.1:n.981+55A>G
ENST00000477310.1:c.2908+55A>G	ENSP00000418996.1:n.2908+55A>G
ENST00000482312.1:n.126A>G
ENST00000483004.1:c.477+55A>G
NM_001710.5:c.1855+55A>G , LRG_136t1:c.1855+55A>G	NP_001701.2:n.1855+55A>G
NM_001710.6:c.1855+55A>G MANE Select	NP_001701.2:n.1855+55A>G