Canonical Allele Identifier: CA363408601

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918404A>T (hg19) ; chr6:g.31950627A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950627A>T , CM000668.2:g.31950627A>T	GRCh38
NC_000006.11:g.31918404A>T , CM000668.1:g.31918404A>T	GRCh37
NC_000006.10:g.32026383A>T	NCBI36
NG_008191.1:g.9684A>T , LRG_136:g.9684A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000452035.7:n.2025A>T
ENST00000483004.2:c.1417A>T	ENSP00000419887.2:p.Lys473Ter
ENST00000698628.1:c.1624+224A>T	ENSP00000513848.1:n.1624+224A>T
ENST00000698629.1:n.1810A>T
ENST00000698630.1:n.2349A>T
ENST00000698631.1:n.2350A>T
ENST00000698632.1:n.3144A>T
ENST00000698633.1:n.3034A>T
ENST00000698636.1:n.1855A>T
ENST00000425368.7:c.1633A>T MANE Select	ENSP00000416561.2:p.Lys545Ter
ENST00000425368.6:c.1633A>T	ENSP00000416561.2:p.Lys545Ter
ENST00000452035.6:n.1848A>T
ENST00000456570.5:c.3139A>T	ENSP00000410815.1:p.Lys1047Ter
ENST00000467360.1:n.759A>T
ENST00000477310.1:c.2686A>T	ENSP00000418996.1:p.Lys896Ter
ENST00000483004.1:c.255A>T
NM_001710.5:c.1633A>T , LRG_136t1:c.1633A>T	NP_001701.2:p.Lys545Ter
NM_001710.6:c.1633A>T MANE Select	NP_001701.2:p.Lys545Ter