Canonical Allele Identifier: CA2678072905
Gene: CFB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31946766_31946773dup , CM000668.2:g.31946766_31946773dup GRCh38
NC_000006.11:g.31914543_31914550dup , CM000668.1:g.31914543_31914550dup GRCh37
NC_000006.10:g.32022522_32022529dup NCBI36
NG_008191.1:g.5823_5830dup , LRG_136:g.5823_5830dup
NG_011730.1:g.24278_24285dup , LRG_26:g.24278_24285dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.475+160_475+167dup
ENST00000483004.2:c.298+160_298+167dup ENSP00000419887.2:n.298+160_298+167dup
ENST00000497841.6:c.298+160_298+167dup ENSP00000513847.1:n.298+160_298+167dup
ENST00000698628.1:c.298+160_298+167dup ENSP00000513848.1:n.298+160_298+167dup
ENST00000698629.1:n.475+160_475+167dup
ENST00000698630.1:n.619_626dup
ENST00000698631.1:n.614_621dup
ENST00000698632.1:n.586_593dup
ENST00000698633.1:n.556_563dup
ENST00000698636.1:n.520+160_520+167dup
ENST00000425368.7:c.298+160_298+167dup MANE Select ENSP00000416561.2:n.298+160_298+167dup
ENST00000425368.6:c.298+160_298+167dup ENSP00000416561.2:n.298+160_298+167dup
ENST00000452035.6:n.298+160_298+167dup
ENST00000456570.5:c.1804+160_1804+167dup ENSP00000410815.1:n.1804+160_1804+167dup
ENST00000460718.5:c.185+160_185+167dup ENSP00000417793.1:n.185+160_185+167dup
ENST00000472581.1:n.705_712dup
ENST00000475617.5:c.298+160_298+167dup ENSP00000420090.1:n.298+160_298+167dup
ENST00000477310.1:c.1352-241_1352-234dup ENSP00000418996.1:n.1352-241_1352-234dup
NM_001710.5:c.298+160_298+167dup , LRG_136t1:c.298+160_298+167dup NP_001701.2:n.298+160_298+167dup
NM_001710.6:c.298+160_298+167dup MANE Select NP_001701.2:n.298+160_298+167dup