Canonical Allele Identifier: CA363409031

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918483A>C (hg19) ; chr6:g.31950706A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950706A>C , CM000668.2:g.31950706A>C	GRCh38
NC_000006.11:g.31918483A>C , CM000668.1:g.31918483A>C	GRCh37
NC_000006.10:g.32026462A>C	NCBI36
NG_008191.1:g.9763A>C , LRG_136:g.9763A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2104A>C
ENST00000483004.2:c.1496A>C	ENSP00000419887.2:p.Glu499Ala
ENST00000698628.1:c.1624+303A>C	ENSP00000513848.1:n.1624+303A>C
ENST00000698629.1:n.1889A>C
ENST00000698630.1:n.2428A>C
ENST00000698631.1:n.2429A>C
ENST00000698632.1:n.3223A>C
ENST00000698633.1:n.3113A>C
ENST00000698636.1:n.1934A>C
ENST00000425368.7:c.1712A>C MANE Select	ENSP00000416561.2:p.Glu571Ala
ENST00000425368.6:c.1712A>C	ENSP00000416561.2:p.Glu571Ala
ENST00000456570.5:c.3218A>C	ENSP00000410815.1:p.Glu1073Ala
ENST00000467360.1:n.838A>C
ENST00000477310.1:c.2765A>C	ENSP00000418996.1:p.Glu922Ala
ENST00000483004.1:c.334A>C
NM_001710.5:c.1712A>C , LRG_136t1:c.1712A>C	NP_001701.2:p.Glu571Ala
NM_001710.6:c.1712A>C MANE Select	NP_001701.2:p.Glu571Ala