Canonical Allele Identifier: CA1619378310
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950400G= , CM000668.2:g.31950400G= GRCh38
NC_000006.11:g.31918177G= , CM000668.1:g.31918177G= GRCh37
NC_000006.10:g.32026156G= NCBI36
NG_008191.1:g.9457G= , LRG_136:g.9457G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.1798G=
ENST00000483004.2:c.1409-219G= ENSP00000419887.2:n.1409-219G=
ENST00000698628.1:c.1621G= ENSP00000513848.1:p.Val541=
ENST00000698629.1:n.1798G=
ENST00000698630.1:n.2337G=
ENST00000698631.1:n.2338G=
ENST00000698632.1:n.2917G=
ENST00000698633.1:n.2807G=
ENST00000698636.1:n.1843G=
ENST00000425368.7:c.1621G= MANE Select ENSP00000416561.2:p.Val541=
ENST00000425368.6:c.1621G= ENSP00000416561.2:p.Val541=
ENST00000452035.6:n.1621G=
ENST00000456570.5:c.3127G= ENSP00000410815.1:p.Val1043=
ENST00000467360.1:n.532G=
ENST00000477310.1:c.2674G= ENSP00000418996.1:p.Val892=
ENST00000483004.1:c.247-219G=
NM_001710.5:c.1621G= , LRG_136t1:c.1621G= NP_001701.2:p.Val541=
NM_001710.6:c.1621G= MANE Select NP_001701.2:p.Val541=