Canonical Allele Identifier: CA1619378575
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950703C= , CM000668.2:g.31950703C= GRCh38
NC_000006.11:g.31918480C= , CM000668.1:g.31918480C= GRCh37
NC_000006.10:g.32026459C= NCBI36
NG_008191.1:g.9760C= , LRG_136:g.9760C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.2101C=
ENST00000483004.2:c.1493C= ENSP00000419887.2:p.Pro498=
ENST00000698628.1:c.1624+300C= ENSP00000513848.1:n.1624+300C=
ENST00000698629.1:n.1886C=
ENST00000698630.1:n.2425C=
ENST00000698631.1:n.2426C=
ENST00000698632.1:n.3220C=
ENST00000698633.1:n.3110C=
ENST00000698636.1:n.1931C=
ENST00000425368.7:c.1709C= MANE Select ENSP00000416561.2:p.Pro570=
ENST00000425368.6:c.1709C= ENSP00000416561.2:p.Pro570=
ENST00000456570.5:c.3215C= ENSP00000410815.1:p.Pro1072=
ENST00000467360.1:n.835C=
ENST00000477310.1:c.2762C= ENSP00000418996.1:p.Pro921=
ENST00000483004.1:c.331C=
NM_001710.5:c.1709C= , LRG_136t1:c.1709C= NP_001701.2:p.Pro570=
NM_001710.6:c.1709C= MANE Select NP_001701.2:p.Pro570=