Canonical Allele Identifier: CA136897447

Gene: CFB

Linked Data

• dbSNP Id: rs927961438
• gnomAD v3: 6-31950487-C-A
• gnomAD v4: 6-31950487-C-A
• MyVariant Identifiers: chr6:g.31950487C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31950487C>A , CM000668.2:g.31950487C>A	GRCh38
NC_000006.11:g.31918264C>A , CM000668.1:g.31918264C>A	GRCh37
NC_000006.10:g.32026243C>A	NCBI36
NG_008191.1:g.9544C>A , LRG_136:g.9544C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452035.7:n.1885C>A
ENST00000483004.2:c.1409-132C>A	ENSP00000419887.2:n.1409-132C>A
ENST00000698628.1:c.1624+84C>A	ENSP00000513848.1:n.1624+84C>A
ENST00000698629.1:n.1801+84C>A
ENST00000698630.1:n.2340+84C>A
ENST00000698631.1:n.2341+84C>A
ENST00000698632.1:n.3004C>A
ENST00000698633.1:n.2894C>A
ENST00000698636.1:n.1846+84C>A
ENST00000425368.7:c.1624+84C>A MANE Select	ENSP00000416561.2:n.1624+84C>A
ENST00000425368.6:c.1624+84C>A	ENSP00000416561.2:n.1624+84C>A
ENST00000452035.6:n.1708C>A
ENST00000456570.5:c.3130+84C>A	ENSP00000410815.1:n.3130+84C>A
ENST00000467360.1:n.619C>A
ENST00000477310.1:c.2677+84C>A	ENSP00000418996.1:n.2677+84C>A
ENST00000483004.1:c.247-132C>A
NM_001710.5:c.1624+84C>A , LRG_136t1:c.1624+84C>A	NP_001701.2:n.1624+84C>A
NM_001710.6:c.1624+84C>A MANE Select	NP_001701.2:n.1624+84C>A