Canonical Allele Identifier: CA363410112

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918707C>A (hg19) ; chr6:g.31950930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950930C>A , CM000668.2:g.31950930C>A	GRCh38
NC_000006.11:g.31918707C>A , CM000668.1:g.31918707C>A	GRCh37
NC_000006.10:g.32026686C>A	NCBI36
NG_008191.1:g.9987C>A , LRG_136:g.9987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2328C>A
ENST00000483004.2:c.1625C>A	ENSP00000419887.2:p.Thr542Asn
ENST00000698628.1:c.1625-214C>A	ENSP00000513848.1:n.1625-214C>A
ENST00000698629.1:n.2113C>A
ENST00000698630.1:n.2557C>A
ENST00000698631.1:n.2558C>A
ENST00000698632.1:n.3447C>A
ENST00000698633.1:n.3337C>A
ENST00000425368.7:c.1841C>A MANE Select	ENSP00000416561.2:p.Thr614Asn
ENST00000425368.6:c.1841C>A	ENSP00000416561.2:p.Thr614Asn
ENST00000456570.5:c.3347C>A	ENSP00000410815.1:p.Thr1116Asn
ENST00000467360.1:n.967C>A
ENST00000477310.1:c.2894C>A	ENSP00000418996.1:p.Thr965Asn
ENST00000482312.1:n.57C>A
ENST00000483004.1:c.463C>A
NM_001710.5:c.1841C>A , LRG_136t1:c.1841C>A	NP_001701.2:p.Thr614Asn
NM_001710.6:c.1841C>A MANE Select	NP_001701.2:p.Thr614Asn