Canonical Allele Identifier: CA1619374681
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31946344G= , CM000668.2:g.31946344G= GRCh38
NC_000006.11:g.31914121G= , CM000668.1:g.31914121G= GRCh37
NC_000006.10:g.32022100G= NCBI36
NG_008191.1:g.5401G= , LRG_136:g.5401G=
NG_011730.1:g.23856G= , LRG_26:g.23856G=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.242-29G=
ENST00000483004.2:c.65-29G= ENSP00000419887.2:n.65-29G=
ENST00000497841.6:c.65-29G= ENSP00000513847.1:n.65-29G=
ENST00000698628.1:c.65-29G= ENSP00000513848.1:n.65-29G=
ENST00000698629.1:n.242-29G=
ENST00000698630.1:n.226-29G=
ENST00000698631.1:n.221-29G=
ENST00000698632.1:n.193-29G=
ENST00000698633.1:n.163-29G=
ENST00000698636.1:n.287-29G=
ENST00000425368.7:c.65-29G= MANE Select ENSP00000416561.2:n.65-29G=
ENST00000425368.6:c.65-29G= ENSP00000416561.2:n.65-29G=
ENST00000452035.6:n.65-29G=
ENST00000456570.5:c.1571-29G= ENSP00000410815.1:n.1571-29G=
ENST00000460718.5:c.64+59G= ENSP00000417793.1:n.64+59G=
ENST00000472581.1:n.312-29G=
ENST00000475617.5:c.65-29G= ENSP00000420090.1:n.65-29G=
ENST00000477310.1:c.1352-663G= ENSP00000418996.1:n.1352-663G=
NM_001710.5:c.65-29G= , LRG_136t1:c.65-29G= NP_001701.2:n.65-29G=
NM_001710.6:c.65-29G= MANE Select NP_001701.2:n.65-29G=