Canonical Allele Identifier: CA449811683

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914184C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946407C>G , CM000668.2:g.31946407C>G	GRCh38
NC_000006.11:g.31914184C>G , CM000668.1:g.31914184C>G	GRCh37
NC_000006.10:g.32022163C>G	NCBI36
NG_008191.1:g.5464C>G , LRG_136:g.5464C>G
NG_011730.1:g.23919C>G , LRG_26:g.23919C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.276C>G
ENST00000483004.2:c.99C>G	ENSP00000419887.2:p.Pro33=
ENST00000497841.6:c.99C>G	ENSP00000513847.1:p.Pro33=
ENST00000698628.1:c.99C>G	ENSP00000513848.1:p.Pro33=
ENST00000698629.1:n.276C>G
ENST00000698630.1:n.260C>G
ENST00000698631.1:n.255C>G
ENST00000698632.1:n.227C>G
ENST00000698633.1:n.197C>G
ENST00000698636.1:n.321C>G
ENST00000425368.7:c.99C>G MANE Select	ENSP00000416561.2:p.Pro33=
ENST00000425368.6:c.99C>G	ENSP00000416561.2:p.Pro33=
ENST00000452035.6:n.99C>G
ENST00000456570.5:c.1605C>G	ENSP00000410815.1:p.Pro535=
ENST00000460718.5:c.65-79C>G	ENSP00000417793.1:n.65-79C>G
ENST00000472581.1:n.346C>G
ENST00000475617.5:c.99C>G	ENSP00000420090.1:p.Pro33=
ENST00000477310.1:c.1352-600C>G	ENSP00000418996.1:n.1352-600C>G
NM_001710.5:c.99C>G , LRG_136t1:c.99C>G	NP_001701.2:p.Pro33=
NM_001710.6:c.99C>G MANE Select	NP_001701.2:p.Pro33=