Canonical Allele Identifier: CA449811893

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914322G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946545G>C , CM000668.2:g.31946545G>C	GRCh38
NC_000006.11:g.31914322G>C , CM000668.1:g.31914322G>C	GRCh37
NC_000006.10:g.32022301G>C	NCBI36
NG_008191.1:g.5602G>C , LRG_136:g.5602G>C
NG_011730.1:g.24057G>C , LRG_26:g.24057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.414G>C
ENST00000483004.2:c.237G>C	ENSP00000419887.2:p.Thr79=
ENST00000497841.6:c.237G>C	ENSP00000513847.1:p.Thr79=
ENST00000698628.1:c.237G>C	ENSP00000513848.1:p.Thr79=
ENST00000698629.1:n.414G>C
ENST00000698630.1:n.398G>C
ENST00000698631.1:n.393G>C
ENST00000698632.1:n.365G>C
ENST00000698633.1:n.335G>C
ENST00000698636.1:n.459G>C
ENST00000425368.7:c.237G>C MANE Select	ENSP00000416561.2:p.Thr79=
ENST00000425368.6:c.237G>C	ENSP00000416561.2:p.Thr79=
ENST00000452035.6:n.237G>C
ENST00000456570.5:c.1743G>C	ENSP00000410815.1:p.Thr581=
ENST00000460718.5:c.124G>C	ENSP00000417793.1:p.Gly42Arg
ENST00000472581.1:n.484G>C
ENST00000475617.5:c.237G>C	ENSP00000420090.1:p.Thr79=
ENST00000477310.1:c.1352-462G>C	ENSP00000418996.1:n.1352-462G>C
NM_001710.5:c.237G>C , LRG_136t1:c.237G>C	NP_001701.2:p.Thr79=
NM_001710.6:c.237G>C MANE Select	NP_001701.2:p.Thr79=