Canonical Allele Identifier: CA363387476

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31914039T>A (hg19) ; chr6:g.31946262T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946262T>A , CM000668.2:g.31946262T>A	GRCh38
NC_000006.11:g.31914039T>A , CM000668.1:g.31914039T>A	GRCh37
NC_000006.10:g.32022018T>A	NCBI36
NG_008191.1:g.5319T>A , LRG_136:g.5319T>A
NG_011730.1:g.23774T>A , LRG_26:g.23774T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.218T>A
ENST00000483004.2:c.41T>A	ENSP00000419887.2:p.Phe14Tyr
ENST00000497841.6:c.41T>A	ENSP00000513847.1:p.Phe14Tyr
ENST00000698628.1:c.41T>A	ENSP00000513848.1:p.Phe14Tyr
ENST00000698629.1:n.218T>A
ENST00000698630.1:n.202T>A
ENST00000698631.1:n.197T>A
ENST00000698632.1:n.169T>A
ENST00000698633.1:n.139T>A
ENST00000698636.1:n.263T>A
ENST00000425368.7:c.41T>A MANE Select	ENSP00000416561.2:p.Phe14Tyr
ENST00000425368.6:c.41T>A	ENSP00000416561.2:p.Phe14Tyr
ENST00000452035.6:n.41T>A
ENST00000456570.5:c.1571-111T>A	ENSP00000410815.1:n.1571-111T>A
ENST00000460718.5:c.41T>A	ENSP00000417793.1:p.Phe14Tyr
ENST00000472581.1:n.288T>A
ENST00000475617.5:c.41T>A	ENSP00000420090.1:p.Phe14Tyr
ENST00000477310.1:c.1352-745T>A	ENSP00000418996.1:n.1352-745T>A
NM_001710.5:c.41T>A , LRG_136t1:c.41T>A	NP_001701.2:p.Phe14Tyr
NM_001710.6:c.41T>A MANE Select	NP_001701.2:p.Phe14Tyr