Canonical Allele Identifier: CA2678073805
Gene: CFB HGNC NCBI

Linked Data

gnomAD v4: 6-31950528-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950528A>G , CM000668.2:g.31950528A>G GRCh38
NC_000006.11:g.31918305A>G , CM000668.1:g.31918305A>G GRCh37
NC_000006.10:g.32026284A>G NCBI36
NG_008191.1:g.9585A>G , LRG_136:g.9585A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.1926A>G
ENST00000483004.2:c.1409-91A>G ENSP00000419887.2:n.1409-91A>G
ENST00000698628.1:c.1624+125A>G ENSP00000513848.1:n.1624+125A>G
ENST00000698629.1:n.1802-91A>G
ENST00000698630.1:n.2341-91A>G
ENST00000698631.1:n.2342-91A>G
ENST00000698632.1:n.3045A>G
ENST00000698633.1:n.2935A>G
ENST00000698636.1:n.1847-91A>G
ENST00000425368.7:c.1625-91A>G MANE Select ENSP00000416561.2:n.1625-91A>G
ENST00000425368.6:c.1625-91A>G ENSP00000416561.2:n.1625-91A>G
ENST00000452035.6:n.1749A>G
ENST00000456570.5:c.3131-91A>G ENSP00000410815.1:n.3131-91A>G
ENST00000467360.1:n.660A>G
ENST00000477310.1:c.2678-91A>G ENSP00000418996.1:n.2678-91A>G
ENST00000483004.1:c.247-91A>G
NM_001710.5:c.1625-91A>G , LRG_136t1:c.1625-91A>G NP_001701.2:n.1625-91A>G
NM_001710.6:c.1625-91A>G MANE Select NP_001701.2:n.1625-91A>G