Canonical Allele Identifier: CA1619379511
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31951834_31951837delinsAATT , CM000668.2:g.31951834_31951837delinsAATT GRCh38
NC_000006.11:g.31919611_31919614delinsAATT , CM000668.1:g.31919611_31919614delinsAATT GRCh37
NC_000006.10:g.32027590_32027593delinsAATT NCBI36
NG_008191.1:g.10891_10894delinsAATT , LRG_136:g.10891_10894delinsAATT

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.2574-41_2574-38delinsAATT
ENST00000483004.2:c.1924-41_1924-38delinsAATT ENSP00000419887.2:n.1924-41_1924-38delins...
ENST00000698628.1:c.1909-41_1909-38delinsAATT ENSP00000513848.1:n.1909-41_1909-38delins...
ENST00000698629.1:n.2359-41_2359-38delinsAATT
ENST00000698630.1:n.2856-41_2856-38delinsAATT
ENST00000698631.1:n.2857-41_2857-38delinsAATT
ENST00000698632.1:n.3945-41_3945-38delinsAATT
ENST00000698633.1:n.3835-41_3835-38delinsAATT
ENST00000425368.7:c.2140-41_2140-38delinsAATT MANE Select ENSP00000416561.2:n.2140-41_2140-38delins...
ENST00000425368.6:c.2140-41_2140-38delinsAATT ENSP00000416561.2:n.2140-41_2140-38delins...
ENST00000456570.5:c.3646-41_3646-38delinsAATT ENSP00000410815.1:n.3646-41_3646-38delins...
ENST00000477310.1:c.3193-41_3193-38delinsAATT ENSP00000418996.1:n.3193-41_3193-38delins...
ENST00000482312.1:n.555-41_555-38delinsAATT
ENST00000483004.1:c.762-41_762-38delinsAATT
ENST00000498317.1:c.339_342delinsAATT
NM_001710.5:c.2140-41_2140-38delinsAATT , LRG_136t1:c.2140-41_2140-38delinsAATT NP_001701.2:n.2140-41_2140-38delinsAATT
NM_001710.6:c.2140-41_2140-38delinsAATT MANE Select NP_001701.2:n.2140-41_2140-38delinsAATT