Canonical Allele Identifier: CA363408817

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918444A>T (hg19) ; chr6:g.31950667A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950667A>T , CM000668.2:g.31950667A>T	GRCh38
NC_000006.11:g.31918444A>T , CM000668.1:g.31918444A>T	GRCh37
NC_000006.10:g.32026423A>T	NCBI36
NG_008191.1:g.9724A>T , LRG_136:g.9724A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2065A>T
ENST00000483004.2:c.1457A>T	ENSP00000419887.2:p.Asn486Ile
ENST00000698628.1:c.1624+264A>T	ENSP00000513848.1:n.1624+264A>T
ENST00000698629.1:n.1850A>T
ENST00000698630.1:n.2389A>T
ENST00000698631.1:n.2390A>T
ENST00000698632.1:n.3184A>T
ENST00000698633.1:n.3074A>T
ENST00000698636.1:n.1895A>T
ENST00000425368.7:c.1673A>T MANE Select	ENSP00000416561.2:p.Asn558Ile
ENST00000425368.6:c.1673A>T	ENSP00000416561.2:p.Asn558Ile
ENST00000456570.5:c.3179A>T	ENSP00000410815.1:p.Asn1060Ile
ENST00000467360.1:n.799A>T
ENST00000477310.1:c.2726A>T	ENSP00000418996.1:p.Asn909Ile
ENST00000483004.1:c.295A>T
NM_001710.5:c.1673A>T , LRG_136t1:c.1673A>T	NP_001701.2:p.Asn558Ile
NM_001710.6:c.1673A>T MANE Select	NP_001701.2:p.Asn558Ile