Canonical Allele Identifier: CA363409079

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918492A>C (hg19) ; chr6:g.31950715A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950715A>C , CM000668.2:g.31950715A>C	GRCh38
NC_000006.11:g.31918492A>C , CM000668.1:g.31918492A>C	GRCh37
NC_000006.10:g.32026471A>C	NCBI36
NG_008191.1:g.9772A>C , LRG_136:g.9772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2113A>C
ENST00000483004.2:c.1505A>C	ENSP00000419887.2:p.Asp502Ala
ENST00000698628.1:c.1624+312A>C	ENSP00000513848.1:n.1624+312A>C
ENST00000698629.1:n.1898A>C
ENST00000698630.1:n.2437A>C
ENST00000698631.1:n.2438A>C
ENST00000698632.1:n.3232A>C
ENST00000698633.1:n.3122A>C
ENST00000698636.1:n.1943A>C
ENST00000425368.7:c.1721A>C MANE Select	ENSP00000416561.2:p.Asp574Ala
ENST00000425368.6:c.1721A>C	ENSP00000416561.2:p.Asp574Ala
ENST00000456570.5:c.3227A>C	ENSP00000410815.1:p.Asp1076Ala
ENST00000467360.1:n.847A>C
ENST00000477310.1:c.2774A>C	ENSP00000418996.1:p.Asp925Ala
ENST00000483004.1:c.343A>C
NM_001710.5:c.1721A>C , LRG_136t1:c.1721A>C	NP_001701.2:p.Asp574Ala
NM_001710.6:c.1721A>C MANE Select	NP_001701.2:p.Asp574Ala