Canonical Allele Identifier: CA363387634

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914062G>C (hg19) ; chr6:g.31946285G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946285G>C , CM000668.2:g.31946285G>C	GRCh38
NC_000006.11:g.31914062G>C , CM000668.1:g.31914062G>C	GRCh37
NC_000006.10:g.32022041G>C	NCBI36
NG_008191.1:g.5342G>C , LRG_136:g.5342G>C
NG_011730.1:g.23797G>C , LRG_26:g.23797G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.241G>C
ENST00000483004.2:c.64G>C	ENSP00000419887.2:p.Gly22Arg
ENST00000497841.6:c.64G>C	ENSP00000513847.1:p.Gly22Arg
ENST00000698628.1:c.64G>C	ENSP00000513848.1:p.Gly22Arg
ENST00000698629.1:n.241G>C
ENST00000698630.1:n.225G>C
ENST00000698631.1:n.220G>C
ENST00000698632.1:n.192G>C
ENST00000698633.1:n.162G>C
ENST00000698636.1:n.286G>C
ENST00000425368.7:c.64G>C MANE Select	ENSP00000416561.2:p.Gly22Arg
ENST00000425368.6:c.64G>C	ENSP00000416561.2:p.Gly22Arg
ENST00000452035.6:n.64G>C
ENST00000456570.5:c.1571-88G>C	ENSP00000410815.1:n.1571-88G>C
ENST00000460718.5:c.64G>C	ENSP00000417793.1:p.Val22Leu
ENST00000472581.1:n.311G>C
ENST00000475617.5:c.64G>C	ENSP00000420090.1:p.Gly22Arg
ENST00000477310.1:c.1352-722G>C	ENSP00000418996.1:n.1352-722G>C
NM_001710.5:c.64G>C , LRG_136t1:c.64G>C	NP_001701.2:p.Gly22Arg
NM_001710.6:c.64G>C MANE Select	NP_001701.2:p.Gly22Arg