Canonical Allele Identifier: CA136897254

Gene: CFB

Linked Data

• dbSNP Id: rs878990414
• MyVariant Identifiers: chr6:g.31918184A>G (hg19) ; chr6:g.31950407A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950407A>G , CM000668.2:g.31950407A>G	GRCh38
NC_000006.11:g.31918184A>G , CM000668.1:g.31918184A>G	GRCh37
NC_000006.10:g.32026163A>G	NCBI36
NG_008191.1:g.9464A>G , LRG_136:g.9464A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.1805A>G
ENST00000483004.2:c.1409-212A>G	ENSP00000419887.2:n.1409-212A>G
ENST00000698628.1:c.1624+4A>G	ENSP00000513848.1:n.1624+4A>G
ENST00000698629.1:n.1801+4A>G
ENST00000698630.1:n.2340+4A>G
ENST00000698631.1:n.2341+4A>G
ENST00000698632.1:n.2924A>G
ENST00000698633.1:n.2814A>G
ENST00000698636.1:n.1846+4A>G
ENST00000425368.7:c.1624+4A>G MANE Select	ENSP00000416561.2:n.1624+4A>G
ENST00000425368.6:c.1624+4A>G	ENSP00000416561.2:n.1624+4A>G
ENST00000452035.6:n.1628A>G
ENST00000456570.5:c.3130+4A>G	ENSP00000410815.1:n.3130+4A>G
ENST00000467360.1:n.539A>G
ENST00000477310.1:c.2677+4A>G	ENSP00000418996.1:n.2677+4A>G
ENST00000483004.1:c.247-212A>G
NM_001710.5:c.1624+4A>G , LRG_136t1:c.1624+4A>G	NP_001701.2:n.1624+4A>G
NM_001710.6:c.1624+4A>G MANE Select	NP_001701.2:n.1624+4A>G