Canonical Allele Identifier: CA363409204

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918513A>G (hg19) ; chr6:g.31950736A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950736A>G , CM000668.2:g.31950736A>G	GRCh38
NC_000006.11:g.31918513A>G , CM000668.1:g.31918513A>G	GRCh37
NC_000006.10:g.32026492A>G	NCBI36
NG_008191.1:g.9793A>G , LRG_136:g.9793A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2134A>G
ENST00000483004.2:c.1526A>G	ENSP00000419887.2:p.Lys509Arg
ENST00000698628.1:c.1624+333A>G	ENSP00000513848.1:n.1624+333A>G
ENST00000698629.1:n.1919A>G
ENST00000698630.1:n.2458A>G
ENST00000698631.1:n.2459A>G
ENST00000698632.1:n.3253A>G
ENST00000698633.1:n.3143A>G
ENST00000698636.1:n.1964A>G
ENST00000425368.7:c.1742A>G MANE Select	ENSP00000416561.2:p.Lys581Arg
ENST00000425368.6:c.1742A>G	ENSP00000416561.2:p.Lys581Arg
ENST00000456570.5:c.3248A>G	ENSP00000410815.1:p.Lys1083Arg
ENST00000467360.1:n.868A>G
ENST00000477310.1:c.2795A>G	ENSP00000418996.1:p.Lys932Arg
ENST00000483004.1:c.364A>G
NM_001710.5:c.1742A>G , LRG_136t1:c.1742A>G	NP_001701.2:p.Lys581Arg
NM_001710.6:c.1742A>G MANE Select	NP_001701.2:p.Lys581Arg