Canonical Allele Identifier: CA2678072754

Gene: CFB

Linked Data

• gnomAD v4: 6-31946728-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946728T>C , CM000668.2:g.31946728T>C	GRCh38
NC_000006.11:g.31914505T>C , CM000668.1:g.31914505T>C	GRCh37
NC_000006.10:g.32022484T>C	NCBI36
NG_008191.1:g.5785T>C , LRG_136:g.5785T>C
NG_011730.1:g.24240T>C , LRG_26:g.24240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.475+122T>C
ENST00000483004.2:c.298+122T>C	ENSP00000419887.2:n.298+122T>C
ENST00000497841.6:c.298+122T>C	ENSP00000513847.1:n.298+122T>C
ENST00000698628.1:c.298+122T>C	ENSP00000513848.1:n.298+122T>C
ENST00000698629.1:n.475+122T>C
ENST00000698630.1:n.581T>C
ENST00000698631.1:n.576T>C
ENST00000698632.1:n.548T>C
ENST00000698633.1:n.518T>C
ENST00000698636.1:n.520+122T>C
ENST00000425368.7:c.298+122T>C MANE Select	ENSP00000416561.2:n.298+122T>C
ENST00000425368.6:c.298+122T>C	ENSP00000416561.2:n.298+122T>C
ENST00000452035.6:n.298+122T>C
ENST00000456570.5:c.1804+122T>C	ENSP00000410815.1:n.1804+122T>C
ENST00000460718.5:c.185+122T>C	ENSP00000417793.1:n.185+122T>C
ENST00000472581.1:n.667T>C
ENST00000475617.5:c.298+122T>C	ENSP00000420090.1:n.298+122T>C
ENST00000477310.1:c.1352-279T>C	ENSP00000418996.1:n.1352-279T>C
NM_001710.5:c.298+122T>C , LRG_136t1:c.298+122T>C	NP_001701.2:n.298+122T>C
NM_001710.6:c.298+122T>C MANE Select	NP_001701.2:n.298+122T>C