Canonical Allele Identifier: CA1619378302
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950391A= , CM000668.2:g.31950391A= GRCh38
NC_000006.11:g.31918168A= , CM000668.1:g.31918168A= GRCh37
NC_000006.10:g.32026147A= NCBI36
NG_008191.1:g.9448A= , LRG_136:g.9448A=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.1789A=
ENST00000483004.2:c.1409-228A= ENSP00000419887.2:n.1409-228A=
ENST00000698628.1:c.1612A= ENSP00000513848.1:p.Lys538=
ENST00000698629.1:n.1789A=
ENST00000698630.1:n.2328A=
ENST00000698631.1:n.2329A=
ENST00000698632.1:n.2908A=
ENST00000698633.1:n.2798A=
ENST00000698636.1:n.1834A=
ENST00000425368.7:c.1612A= MANE Select ENSP00000416561.2:p.Lys538=
ENST00000425368.6:c.1612A= ENSP00000416561.2:p.Lys538=
ENST00000452035.6:n.1612A=
ENST00000456570.5:c.3118A= ENSP00000410815.1:p.Lys1040=
ENST00000467360.1:n.523A=
ENST00000477310.1:c.2665A= ENSP00000418996.1:p.Lys889=
ENST00000483004.1:c.247-228A=
NM_001710.5:c.1612A= , LRG_136t1:c.1612A= NP_001701.2:p.Lys538=
NM_001710.6:c.1612A= MANE Select NP_001701.2:p.Lys538=