Canonical Allele Identifier: CA566693427

Gene: CFB

Linked Data

• dbSNP Id: rs1442976724
• gnomAD v2: 6-31914535-A-G
• gnomAD v3: 6-31946758-A-G
• gnomAD v4: 6-31946758-A-G
• MyVariant Identifiers: chr6:g.31914535A>G (hg19) ; chr6:g.31946758A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31946758A>G , CM000668.2:g.31946758A>G	GRCh38
NC_000006.11:g.31914535A>G , CM000668.1:g.31914535A>G	GRCh37
NC_000006.10:g.32022514A>G	NCBI36
NG_008191.1:g.5815A>G , LRG_136:g.5815A>G
NG_011730.1:g.24270A>G , LRG_26:g.24270A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.475+152A>G
ENST00000483004.2:c.298+152A>G	ENSP00000419887.2:n.298+152A>G
ENST00000497841.6:c.298+152A>G	ENSP00000513847.1:n.298+152A>G
ENST00000698628.1:c.298+152A>G	ENSP00000513848.1:n.298+152A>G
ENST00000698629.1:n.475+152A>G
ENST00000698630.1:n.611A>G
ENST00000698631.1:n.606A>G
ENST00000698632.1:n.578A>G
ENST00000698633.1:n.548A>G
ENST00000698636.1:n.520+152A>G
ENST00000425368.7:c.298+152A>G MANE Select	ENSP00000416561.2:n.298+152A>G
ENST00000425368.6:c.298+152A>G	ENSP00000416561.2:n.298+152A>G
ENST00000452035.6:n.298+152A>G
ENST00000456570.5:c.1804+152A>G	ENSP00000410815.1:n.1804+152A>G
ENST00000460718.5:c.185+152A>G	ENSP00000417793.1:n.185+152A>G
ENST00000472581.1:n.697A>G
ENST00000475617.5:c.298+152A>G	ENSP00000420090.1:n.298+152A>G
ENST00000477310.1:c.1352-249A>G	ENSP00000418996.1:n.1352-249A>G
NM_001710.5:c.298+152A>G , LRG_136t1:c.298+152A>G	NP_001701.2:n.298+152A>G
NM_001710.6:c.298+152A>G MANE Select	NP_001701.2:n.298+152A>G