Canonical Allele Identifier: CA449812106

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918451C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950674C>T , CM000668.2:g.31950674C>T	GRCh38
NC_000006.11:g.31918451C>T , CM000668.1:g.31918451C>T	GRCh37
NC_000006.10:g.32026430C>T	NCBI36
NG_008191.1:g.9731C>T , LRG_136:g.9731C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2072C>T
ENST00000483004.2:c.1464C>T	ENSP00000419887.2:p.Asn488=
ENST00000698628.1:c.1624+271C>T	ENSP00000513848.1:n.1624+271C>T
ENST00000698629.1:n.1857C>T
ENST00000698630.1:n.2396C>T
ENST00000698631.1:n.2397C>T
ENST00000698632.1:n.3191C>T
ENST00000698633.1:n.3081C>T
ENST00000698636.1:n.1902C>T
ENST00000425368.7:c.1680C>T MANE Select	ENSP00000416561.2:p.Asn560=
ENST00000425368.6:c.1680C>T	ENSP00000416561.2:p.Asn560=
ENST00000456570.5:c.3186C>T	ENSP00000410815.1:p.Asn1062=
ENST00000467360.1:n.806C>T
ENST00000477310.1:c.2733C>T	ENSP00000418996.1:p.Asn911=
ENST00000483004.1:c.302C>T
NM_001710.5:c.1680C>T , LRG_136t1:c.1680C>T	NP_001701.2:p.Asn560=
NM_001710.6:c.1680C>T MANE Select	NP_001701.2:p.Asn560=