Canonical Allele Identifier: CA1619379527
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31951858C= , CM000668.2:g.31951858C= GRCh38
NC_000006.11:g.31919635C= , CM000668.1:g.31919635C= GRCh37
NC_000006.10:g.32027614C= NCBI36
NG_008191.1:g.10915C= , LRG_136:g.10915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.2574-17C=
ENST00000483004.2:c.1924-17C= ENSP00000419887.2:n.1924-17C=
ENST00000698628.1:c.1909-17C= ENSP00000513848.1:n.1909-17C=
ENST00000698629.1:n.2359-17C=
ENST00000698630.1:n.2856-17C=
ENST00000698631.1:n.2857-17C=
ENST00000698632.1:n.3945-17C=
ENST00000698633.1:n.3835-17C=
ENST00000425368.7:c.2140-17C= MANE Select ENSP00000416561.2:n.2140-17C=
ENST00000425368.6:c.2140-17C= ENSP00000416561.2:n.2140-17C=
ENST00000456570.5:c.3646-17C= ENSP00000410815.1:n.3646-17C=
ENST00000477310.1:c.3193-17C= ENSP00000418996.1:n.3193-17C=
ENST00000482312.1:n.555-17C=
ENST00000483004.1:c.762-17C=
ENST00000498317.1:c.363C=
NM_001710.5:c.2140-17C= , LRG_136t1:c.2140-17C= NP_001701.2:n.2140-17C=
NM_001710.6:c.2140-17C= MANE Select NP_001701.2:n.2140-17C=