Canonical Allele Identifier: CA449812044

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918412C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950635C>T , CM000668.2:g.31950635C>T	GRCh38
NC_000006.11:g.31918412C>T , CM000668.1:g.31918412C>T	GRCh37
NC_000006.10:g.32026391C>T	NCBI36
NG_008191.1:g.9692C>T , LRG_136:g.9692C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2033C>T
ENST00000483004.2:c.1425C>T	ENSP00000419887.2:p.Asp475=
ENST00000698628.1:c.1624+232C>T	ENSP00000513848.1:n.1624+232C>T
ENST00000698629.1:n.1818C>T
ENST00000698630.1:n.2357C>T
ENST00000698631.1:n.2358C>T
ENST00000698632.1:n.3152C>T
ENST00000698633.1:n.3042C>T
ENST00000698636.1:n.1863C>T
ENST00000425368.7:c.1641C>T MANE Select	ENSP00000416561.2:p.Asp547=
ENST00000425368.6:c.1641C>T	ENSP00000416561.2:p.Asp547=
ENST00000452035.6:n.1856C>T
ENST00000456570.5:c.3147C>T	ENSP00000410815.1:p.Asp1049=
ENST00000467360.1:n.767C>T
ENST00000477310.1:c.2694C>T	ENSP00000418996.1:p.Asp898=
ENST00000483004.1:c.263C>T
NM_001710.5:c.1641C>T , LRG_136t1:c.1641C>T	NP_001701.2:p.Asp547=
NM_001710.6:c.1641C>T MANE Select	NP_001701.2:p.Asp547=