Canonical Allele Identifier: CA1619378313
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950406A= , CM000668.2:g.31950406A= GRCh38
NC_000006.11:g.31918183A= , CM000668.1:g.31918183A= GRCh37
NC_000006.10:g.32026162A= NCBI36
NG_008191.1:g.9463A= , LRG_136:g.9463A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.1804A=
ENST00000483004.2:c.1409-213A= ENSP00000419887.2:n.1409-213A=
ENST00000698628.1:c.1624+3A= ENSP00000513848.1:n.1624+3A=
ENST00000698629.1:n.1801+3A=
ENST00000698630.1:n.2340+3A=
ENST00000698631.1:n.2341+3A=
ENST00000698632.1:n.2923A=
ENST00000698633.1:n.2813A=
ENST00000698636.1:n.1846+3A=
ENST00000425368.7:c.1624+3A= MANE Select ENSP00000416561.2:n.1624+3A=
ENST00000425368.6:c.1624+3A= ENSP00000416561.2:n.1624+3A=
ENST00000452035.6:n.1627A=
ENST00000456570.5:c.3130+3A= ENSP00000410815.1:n.3130+3A=
ENST00000467360.1:n.538A=
ENST00000477310.1:c.2677+3A= ENSP00000418996.1:n.2677+3A=
ENST00000483004.1:c.247-213A=
NM_001710.5:c.1624+3A= , LRG_136t1:c.1624+3A= NP_001701.2:n.1624+3A=
NM_001710.6:c.1624+3A= MANE Select NP_001701.2:n.1624+3A=