Canonical Allele Identifier: CA363409418

Gene: CFB

Linked Data

• MyVariant Identifiers: chr6:g.31918539C>G (hg19) ; chr6:g.31950762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950762C>G , CM000668.2:g.31950762C>G	GRCh38
NC_000006.11:g.31918539C>G , CM000668.1:g.31918539C>G	GRCh37
NC_000006.10:g.32026518C>G	NCBI36
NG_008191.1:g.9819C>G , LRG_136:g.9819C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.2160C>G
ENST00000483004.2:c.1552C>G	ENSP00000419887.2:p.Gln518Glu
ENST00000698628.1:c.1624+359C>G	ENSP00000513848.1:n.1624+359C>G
ENST00000698629.1:n.1945C>G
ENST00000698630.1:n.2484C>G
ENST00000698631.1:n.2485C>G
ENST00000698632.1:n.3279C>G
ENST00000698633.1:n.3169C>G
ENST00000698636.1:n.1990C>G
ENST00000425368.7:c.1768C>G MANE Select	ENSP00000416561.2:p.Gln590Glu
ENST00000425368.6:c.1768C>G	ENSP00000416561.2:p.Gln590Glu
ENST00000456570.5:c.3274C>G	ENSP00000410815.1:p.Gln1092Glu
ENST00000467360.1:n.894C>G
ENST00000477310.1:c.2821C>G	ENSP00000418996.1:p.Gln941Glu
ENST00000483004.1:c.390C>G
NM_001710.5:c.1768C>G , LRG_136t1:c.1768C>G	NP_001701.2:p.Gln590Glu
NM_001710.6:c.1768C>G MANE Select	NP_001701.2:p.Gln590Glu