Canonical Allele Identifier: CA449812065

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918427A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950650A>T , CM000668.2:g.31950650A>T	GRCh38
NC_000006.11:g.31918427A>T , CM000668.1:g.31918427A>T	GRCh37
NC_000006.10:g.32026406A>T	NCBI36
NG_008191.1:g.9707A>T , LRG_136:g.9707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2048A>T
ENST00000483004.2:c.1440A>T	ENSP00000419887.2:p.Val480=
ENST00000698628.1:c.1624+247A>T	ENSP00000513848.1:n.1624+247A>T
ENST00000698629.1:n.1833A>T
ENST00000698630.1:n.2372A>T
ENST00000698631.1:n.2373A>T
ENST00000698632.1:n.3167A>T
ENST00000698633.1:n.3057A>T
ENST00000698636.1:n.1878A>T
ENST00000425368.7:c.1656A>T MANE Select	ENSP00000416561.2:p.Val552=
ENST00000425368.6:c.1656A>T	ENSP00000416561.2:p.Val552=
ENST00000456570.5:c.3162A>T	ENSP00000410815.1:p.Val1054=
ENST00000467360.1:n.782A>T
ENST00000477310.1:c.2709A>T	ENSP00000418996.1:p.Val903=
ENST00000483004.1:c.278A>T
NM_001710.5:c.1656A>T , LRG_136t1:c.1656A>T	NP_001701.2:p.Val552=
NM_001710.6:c.1656A>T MANE Select	NP_001701.2:p.Val552=