Canonical Allele Identifier: CA363410198

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918712C>G (hg19) ; chr6:g.31950935C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950935C>G , CM000668.2:g.31950935C>G	GRCh38
NC_000006.11:g.31918712C>G , CM000668.1:g.31918712C>G	GRCh37
NC_000006.10:g.32026691C>G	NCBI36
NG_008191.1:g.9992C>G , LRG_136:g.9992C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2333C>G
ENST00000483004.2:c.1630C>G	ENSP00000419887.2:p.Gln544Glu
ENST00000698628.1:c.1625-209C>G	ENSP00000513848.1:n.1625-209C>G
ENST00000698629.1:n.2118C>G
ENST00000698630.1:n.2562C>G
ENST00000698631.1:n.2563C>G
ENST00000698632.1:n.3452C>G
ENST00000698633.1:n.3342C>G
ENST00000425368.7:c.1846C>G MANE Select	ENSP00000416561.2:p.Gln616Glu
ENST00000425368.6:c.1846C>G	ENSP00000416561.2:p.Gln616Glu
ENST00000456570.5:c.3352C>G	ENSP00000410815.1:p.Gln1118Glu
ENST00000467360.1:n.972C>G
ENST00000477310.1:c.2899C>G	ENSP00000418996.1:p.Gln967Glu
ENST00000482312.1:n.62C>G
ENST00000483004.1:c.468C>G
NM_001710.5:c.1846C>G , LRG_136t1:c.1846C>G	NP_001701.2:p.Gln616Glu
NM_001710.6:c.1846C>G MANE Select	NP_001701.2:p.Gln616Glu